Patent Application
20220119375
The present invention relates to the field of medicinal chemistry and pharmacotherapy. Specifically, the present invention relates to a 3-aryloxy-3-aryl-propylamine compound and uses thereof.
Pain is an unpleasant feeling and emotional experience caused by tissue damage or potential tissue damage. It is a warning signal sent by the body. However, severe or long-term pain causes an unbearable torture on the body and seriously affects the patient's life. Therefore, the International Pain Society has designated October 11 of each year as “Global Pain Day” since 2004.
Pain can be divided into acute pain and chronic pain based on duration time. Acute pain is nociceptive pain usually caused by tissue trauma, while chronic pain is a disease mainly dominated by neuropathic pain. Traditional analgesic drugs mainly comprise opioids and non-steroidal anti-inflammatory drugs. Opioids have strong analgesic effect, but long-term use of opioids is easy to cause tolerance, dependence and addiction, and opioids have adverse effects such as respiratory depression and central sedation. Non-steroidal anti-inflammatory drugs only have moderate analgesic effect, while having adverse effects such as gastrointestinal bleeding and cardiotoxicity, etc.
TRPA1, also known as ANKTM1, is a member of TRP ion channel superfamily. TRPA1 is mainly distributed on the primary sensory neurons of dorsal root nerve (DRG), trigeminal nerve (TG) and vagus nerve (VG), and is expressed in peptide energy neurons having rich neuropeptides CGRP, SP and neurotrophic factor receptor TrkA, and in non-peptidergic neurons co-expressing purinergic receptors P2X3, neurturin, artemin, G protein-coupled receptors in Mrg family, and GFRα1, GFRα2 in GDNF receptor family). From the distribution of human system, TRPA1 is highly expressed in the peripheral nervous system, respiratory system, gastrointestinal system and urinary system. When these organs and tissues have abnormal functions, the expression and function of TRPA1 channels are usually abnormal simultaneously. TRPA1 can convert cold stimulation, chemical stimulation and mechanical stimulation into inward currents, trigger a series of physiological functions, and participate in the formation of various pain sensations.
Inflammation is the defensive response of living tissues with vascular system to injury factors. The stimulation of inflammatory mediators such as prostaglandin, serotonin, bradykinin, etc. is the main cause of local pain caused by inflammation. Inflammatory pain is common problem of certain chronic diseases, and there is still no effective treatment method in the clinic. Animal experiments have shown that TRPA1 is involved in inflammatory response and plays an important role in inflammatory pain. The use of TRA1 specific blockers can significantly reduce the inflammatory pain response in rats. The pathogenesis of asthma and cough has become more and more clear as the research continues. From the current research, TRPA1 plays an important role in the occurrence of asthma and cough. Compounds that induce asthma and cough, either cellular endogenous factors or exogenous factors, can activate TRPA1. TRPA1 antagonists can reduce asthma symptoms and block airway hyper-responsiveness.
Visceral pain, as a main visceral sensation, is often caused by viscera stimulation such as mechanical traction, spasm, ischemia, or inflammation, etc. It is confirmed that TRPA1 is involved in the regulation of visceral hypersensitivity through different visceral hypersensitivity animal models such as colitis, rectal dilatation or stress. Neuropathic pain is a pain syndrome caused by central or peripheral nervous system damage or disease, mainly manifested as allodynia, allodynia, and spontaneous pain. Different from inflammatory pain, neurogenic pain is not related to vascular response of central inflammation, but depends on the damage and dysfunction of nervous system, which is often caused by peripheral nerve damage. In recent years, more and more studies have shown that TRPA1 channel plays an important role in different neurogenic pain, such as diabetic neuropathy and neuropathy caused by chemotherapy drugs. Recent studies have also shown that TRPA1 also has a mediating role in toothache, migraine and other pains. The administration of TRPA1 antagonists can significantly alleviate the pain symptoms.
Since TRPA1 is widely distributed and expressed in the human system, the importance of its function is self-evident. In addition to the physiological functions involved by TRPA1, the development of TRPA1 inhibitor indications reported so far also involves inflammatory bowel disease, chronic obstructive pulmonary disease, antitussive, antipruritic, allergic rhinitis, ear disease, diabetic, urinary incontinence, etc. It is proved that TRPA1 is a new target for pain treatment. There is no commercial drug for TRPA1 target. Pain is a refractory disease.
Therefore, there is an urgent need in the art to develop a medicament targeting TRP, especially TRPA1, to improve therapeutic effect of diseases.
It is an object of the present invention to provide novel compounds which target TRP channel, especially TRPA1, and uses thereof.
In the first aspect of the present invention, it provides a use of a compound of formula I, or a pharmaceutically acceptable salt, or a prodrug thereof in (a) preparing a transient receptor potential channel protein (TRP) inhibitor; or (b) preparing a medicine for preventing and/or treating a disease related to transient receptor potential channel protein (TRP);
wherein,
A is
wherein ring B is a substituted or unsubstituted 5-7 membered carbocyclic ring, a substituted or unsubstituted 5-7 membered heterocyclic ring, substituted or unsubstituted 5-7 membered heteroaryl, substituted or unsubstituted C6-C12 aryl; ring D is substituted or unsubstituted 5-7 membered heteroaryl, substituted or unsubstituted C6-C12 aryl; and when A is substituted or unsubstituted aromatic structure, A contains 1-3 heteroatoms selected from the group consisting of N, O and S;
wherein the heterocyclic ring or heteroaryl contains 1-3 heteroatoms selected from the group consisting of N, O and S;
R1 and R2 are each independently hydrogen, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted C3-C7 cycloalkyl, substituted or unsubstituted C2-C4 acyl, substituted or unsubstituted C2-C6 ester group, or R1, R2 and their linking N atom constitute substituted or unsubstituted C3-C7 heterocycloalkyl; wherein the heterocycloalkyl contains 1-2 N atoms and 0-1 O or S atom;
X is carbon atom, oxygen atom, sulfur atom or nitrogen atom;
Y is carbon atom or nitrogen atom;
at least one of X and Y is heteroatom;
R3 is hydrogen, halogen, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted C3-C7 cycloalkyl;
n is 1, 2, 3, 4 or 5;
“*” represents a chiral carbon atom, and the absolute configuration of the chiral carbon atom is S type;
wherein the “substituted” means that 1-4 (preferably 1, 2, or 3) hydrogen atoms on the group are substituted by a substituent selected from the group consisting of C1-C6 alkyl, C3-C7 cycloalkyl, haloalkyl, halogen, nitro, cyano, hydroxyl, C1-C4 carboxyl, C2-C4 ester group, C2-C4 amide group, C1-C6 alkoxyl, C1-C6 haloalkoxy, benzyl, 5- or 6-membered aryl or heteroaryl (preferably C6 aryl or C5 heteroaryl).
In another preferred embodiment, A is
In another preferred embodiment, A is not naphthalene ring.
In another preferred embodiment, A is substituted or unsubstituted C6-C12 bicyclic heteroaryl, substituted or unsubstituted 5-6 membered heterocycle-bis-phenyl, substituted or unsubstituted 5-6 membered heterocycle-bis-5-6 membered heteroaryl, or substituted or unsubstituted C6-C12 benzoalicyclic group.
In another preferred embodiment, the C6-C12 bicyclic heteroaryl is quinolinyl, isoquinolinyl, phthalimidyl, benzofuranyl, benzothienyl, indolyl, benzooxazolyl, benzothiazolyl, quinoxalinyl, imidazopyridyl or benzimidazolonyl.
In another preferred embodiment, the C6-C12 benzoalicyclic group comprises indanyl, tetrahydronaphthyl or dihydronaphthyl.
In another preferred embodiment, A is substituted or unsubstituted benzofuranyl, benzothienyl, or indanyl.
In another preferred embodiment, at least one of X and Y is heteroatom.
In another preferred embodiment, X is S or O.
In another preferred embodiment, X is S.
In another preferred embodiment, the heteroaryl contains 1-3 heteroatoms selected from the group consisting of N, O and S.
In another preferred embodiment, the
is unsubstituted heteroaryl, or substituted heteroaryl having 1-5 R3 substituents.
In another preferred embodiment, the “substituted” means that one or more (preferably 1, 2, or 3) hydrogen atoms on the group are substituted by a substituent selected from the group consisting of C1-C3 alkyl, C3-C7 cycloalkyl, C1-C3 haloalkyl, halogen, nitro, cyano, hydroxyl, carboxyl, C2-C4 ester group, C2-C4 amide group, C1-C4 alkoxy, C1-C6 haloalkoxy, benzyl, 5- or 6-membered aryl or heteroaryl (preferably C6 aryl or C5 heteroaryl).
In another preferred embodiment, the transient receptor potential channel protein (TRP) is TRPA1.
In another preferred embodiment, A is substituted or unsubstituted C6-C12 bicyclic heteroaryl, substituted or unsubstituted 5-6 membered heterocycle-bis-phenyl, substituted or unsubstituted 5-6 membered heterocycle-bis-5-6 membered heteroaryl, or substituted or unsubstituted C6-C12 benzoalicyclic group.
In another preferred embodiment, R1 and R2 are each independently hydrogen atom, C1-C3 alkyl, or C2-C4 acyl group; or R1, R2 and their linking N atom constitute tetrahydropyrrolyl substituted by carboxyl or C2-C4 ester group.
In another preferred embodiment, R3 is hydrogen atom, halogen, or substituted or unsubstituted C1-C3 alkyl.
In another preferred embodiment, A is quinolinyl, isoquinolinyl, phthalimidyl, benzofuranyl, benzothienyl, indolyl, benzoxazolyl, benzothiazolyl, quinoxalinyl, imidazopyridyl, benzimidazolonyl, indanyl, tetrahydronaphthyl or dihydronaphthyl.
In another preferred embodiment, R1 and R2 are each independently hydrogen, methyl, or acetyl, or R1, R2 and their linking N atom constitute proline group or proline methyl ester group.
In another preferred embodiment, R3 is hydrogen atom, chlorine atom or methyl.
In another preferred embodiment, the compound is selected from the following group:
In another preferred embodiment, the transient receptor potential channel protein (TRP) is TRPA1.
In another preferred embodiment, the disease related to transient receptor potential channel protein (TRP) is selected from the group consisting of pain, epilepsy, inflammation, respiratory disorder, pruritus, urinary tract disorder and inflammatory bowel disease.
In another preferred embodiment, the pain comprises acute inflammatory pain, chronic inflammatory pain, visceral pain, neurogenic pain, fibromyalgia, headache, neuralgia or pain caused by cancer.
In another preferred embodiment, the headache is migraine or muscle tension pain.
In another preferred embodiment, the neuralgia is trigeminal neuralgia, diabetic pain or post-zoster neuralgia.
In another preferred embodiment, the pain is selected from the group consisting of acute pain, fibromyalgia, visceral pain, inflammatory pain, neuralgia, or a combination thereof.
In another preferred embodiment, the other pain is fibromyalgia.
In the second aspect of the present invention, it provides a compound of formula I, or a pharmaceutically acceptable salt, or a prodrug thereof;
wherein,
A is
wherein ring B is a substituted or unsubstituted 5-7 membered carbocyclic ring, a substituted or unsubstituted 5-7 membered heterocyclic ring, substituted or unsubstituted 5-7 membered heteroaryl, substituted or unsubstituted C6-C12 aryl; ring D is substituted or unsubstituted 5-7 membered heteroaryl, substituted or unsubstituted C6-C12 aryl; and when A is substituted or unsubstituted aromatic structure, A contains 1-3 heteroatoms selected from the group consisting of N, O and S;
wherein the heterocyclic ring or heteroaryl contains 1-3 heteroatoms selected from the group consisting of N, O and S;
R1 and R2 are each independently hydrogen, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted C3-C7 cycloalkyl, substituted or unsubstituted C2-C4 acyl, substituted or unsubstituted C2-C6 ester group, or R1, R2 and their linking N atom constitute substituted or unsubstituted C3-C7 heterocycloalkyl; wherein the heterocycloalkyl contains 1-2 N atoms and 0-1 O or S atom;
X is carbon atom, oxygen atom, sulfur atom or nitrogen atom;
Y is carbon atom or nitrogen atom;
at least one of X and Y is heteroatom;
R3 is hydrogen, halogen, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted C3-C7 cycloalkyl;
n is 1, 2, 3, 4 or 5;
“*” represents a chiral carbon atom, and the absolute configuration of the chiral carbon atom is S type;
wherein, the “substituted” means that 1-4 (preferably 1, 2, or 3) hydrogen atoms on the group are substituted by a substituent selected from the group consisting of C1-C6 alkyl, C3-C7 cycloalkyl, C1-C3 haloalkyl, halogen, nitro, cyano, hydroxyl, C1-C4 carboxyl, C2-C4 ester group, C2-C4 amide group, C1-C6 alkoxyl, C1-C6 haloalkoxy, benzyl, 5- or 6-membered aryl or heteroaryl (preferably C6 aryl or C5 heteroaryl).
In another preferred embodiment, A is
In another preferred embodiment, A is not naphthalene ring.
In another preferred embodiment, A is substituted or unsubstituted C6-C12 bicyclic heteroaryl, substituted or unsubstituted 5-6 membered heterocycle-bis-phenyl, substituted or unsubstituted 5-6 membered heterocycle-bis-5-6 membered heteroaryl, or substituted or unsubstituted C6-C12 benzoalicyclic group.
In another preferred embodiment, the C6-C12 bicyclic heteroaryl is quinolinyl, isoquinolinyl, phthalimidyl, benzofuranyl, benzothienyl, indolyl, benzooxazolyl, benzothiazolyl, quinoxalinyl, imidazopyridyl or benzimidazolonyl.
In another preferred embodiment, the C6-C12 benzoalicyclic group comprises indanyl, tetrahydronaphthyl or dihydronaphthyl.
In another preferred embodiment, A is substituted or unsubstituted benzofuranyl, benzothienyl, or indanyl.
In another preferred embodiment, at least one of X and Y is heteroatom.
In another preferred embodiment, X is S or 0.
In another preferred embodiment, X is S.
In another preferred embodiment, the heteroaryl contains 1-3 heteroatoms selected from the group consisting of N, O and S.
In another preferred embodiment, the
is unsubstituted heteroaryl, or substituted heteroaryl having 1-5 R3 substituents.
In another preferred embodiment, the “substituted” means that 1-4 (preferably 1, 2, or 3) hydrogen atoms on the group are substituted by a substituent selected from the group consisting of C1-C3 alkyl, C3-C7 cycloalkyl, C1-C3 haloalkyl, halogen, nitro, cyano, hydroxyl, carboxyl, C2-C4 ester group, C2-C4 amide group, C1-C4 alkoxy, C1-C6 haloalkoxy, benzyl, 5- or 6-membered aryl or heteroaryl (preferably C6 aryl or C5 heteroaryl).
In another preferred embodiment, A is substituted or unsubstituted C6-C12 bicyclic heteroaryl, substituted or unsubstituted 5-6 membered heterocycle-bis-phenyl, substituted or unsubstituted 5-6 membered heterocycle-bis-5-6 membered heteroaryl, or substituted or unsubstituted C6-C12 benzoalicyclic group.
In another preferred embodiment, R1 and R2 are each independently hydrogen atom, C1-C3 alkyl, C2-C4 acyl group; or R1, R2 and their linking N atom constitute tetrahydropyrrolyl substituted by carboxyl or C7-C4 ester group.
In another preferred embodiment, R3 is hydrogen atom, halogen, or substituted or unsubstituted C1-C3 alkyl.
In another preferred embodiment, A is quinolinyl, isoquinolinyl, phthalimidyl, benzofuranyl, benzothienyl, indolyl, benzoxazolyl, benzothiazolyl, quinoxalinyl, imidazopyridyl, benzimidazolonyl, indanyl, tetrahydronaphthyl or dihydronaphthyl.
In another preferred embodiment, R1 and R2 are each independently hydrogen, methyl, or acetyl, or R1, R2 and their linking N atom constitute proline group or proline methyl ester group.
In another preferred embodiment, R3 is hydrogen atom, chlorine atom or methyl.
In another preferred embodiment, the compound is selected from the following group:
In the third aspect of the present invention, it provides a pharmaceutical composition which comprises the compound, or a pharmaceutically acceptable salt, or a prodrug thereof according to the second aspect of the present invention; and a pharmaceutically acceptable carrier.
In the fourth aspect of the present invention, it provides a method for preparing the compound, or a pharmaceutically acceptable salt, or a prodrug thereof according to the second aspect of the present invention, wherein the method comprises: reacting an intermediate of formula II with R1—NH—R2 in an inert solvent, thereby forming the compound:
wherein X, Y, A, R1, R2, R3 and “*” are as defined in the second aspect of the present invention.
In another preferred embodiment, the method comprises the following step:
reacting monofluoro-substituted quinoline or monofluoro-substituted isoquinoline with 3-(methylamino)-1-(thiophen-2-yl)propan-1-ol in an inert solvent, thereby forming a compound of formula IA or IB;
In another preferred embodiment, the method comprises the following step:
wherein X, Y, A, R1, R2, R3 and “*” are as defined in the second aspect of the present invention;
(a) in an inert solvent and in presence of a condensing agent, reacting a compound A-OH with 1-(R3-5-membered heteroaryl)-3-chloro-propanol, thereby forming an intermediate of formula II;
(b) carrying out a reaction selected from the following group to form a compound of formula IC or IE:
(b-1) in an inert solvent, reacting the intermediate of formula II with R1—NH—R2 to form a compound of formula Ic; or
(b-2) in an inert solvent, reacting the intermediate of formula II with phthalimide to form an intermediate of formula III, and subjecting the intermediate of formula III to hydrazinolysis reaction to form the compound of formula Ic; or
(b-3) in an inert solvent, reacting the intermediate of formula II with proline methyl ester to form the compound IE.
In another preferred embodiment, the method further comprises the following step:
(c1) in an inert solvent and in presence of a condensing agent, reacting the compound of formula Ic with acetic acid to form a compound of formula ID;
In another preferred embodiment, the method further comprises the following step:
(c2) in an inert solvent and in presence of a base, subjecting the compound of formula IE to hydrolysis reaction to form a compound of formula IF.
In the fifth aspect of the present invention, it provides an intermediate of formula II or III:
wherein, X, Y, A, R3 and “*” are as defined in the second aspect of the present invention.
In the six aspect of the present invention, it provides a method for preparing the intermediate according to the fifth aspect of the present invention,
wherein X, Y, A, R1, R2, R3 and “*” are as defined in the second aspect of the present invention.
(1) the method comprises:
(i) in an inert solvent and in presence of a condensing agent, reacting compound A-OH with 1-(R3-5-membered heteroaryl)-3-chloro-propanol, thereby forming an intermediate of formula II;
or (2) the method comprises:
(i) in an inert solvent and in presence of a condensing agent, reacting compound A-OH 1-(R3-5-membered heteroaryl)-3-chloro-propanol, thereby forming an intermediate of formula II; and
(ii) in an inert solvent, reacting the intermediate of formula II with phthalimide, thereby forming an intermediate of formula III.
In the seventh aspect of the present invention, it provides a method for non-therapeutically and/or non-diagnostically inhibiting activity of transient receptor potential channel protein in vitro, which comprises contacting a transient receptor potential channel protein or a cell expressing the protein with the compound, or a pharmaceutically acceptable salt, or a prodrug thereof according to the second aspect of present invention, thereby inhibiting activity of transient receptor potential channel protein.
In the eighth aspect of the present invention, it provides a method for inhibiting transient receptor potential channel protein or preventing and/or treating a disease related to transient receptor potential channel protein (TRP), which comprises administering the compound, or a pharmaceutically acceptable salt, or a prodrug thereof according to the second aspect of the present invention to a subject in need of.
It should be understood that, in the present invention, each of the technical features specifically described above and below (such as those in the Examples) can be combined with each other, thereby constituting new or preferred technical solutions which need not be redundantly described one-by-one.
Based on an extensive and intensive research, the inventors have unexpectedly and firstly developed a compound of formula I, or a pharmaceutically acceptable salt, or a prodrug thereof. The experimental results have shown that the compound of present invention have significant inhibitory effect on TRP channels. The compound of present invention can effectively treat a pain and the like related to TRP (especially TRPA1) targets. On this basis, the inventors has completed the present invention.
As used herein, the terms “comprise”, “comprising”, and “containing” are used interchangeably, which not only comprise closed definitions, but also semi-closed and open definitions. In other words, the term comprises “consisting of” and “essentially consisting of”.
As used herein, “R1”, “R1” and “R1” have the same meaning and can be used interchangeably. The other similar definitions have the same meaning.
As used herein, the terms “C1-C6 alkyl” or “C1-C3 alkyl” refer to a linear or branched chain alkyl with 1-6 or 1-3 carbon atoms, such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, or the like.
As used herein, the term “C1-C6 alkoxy” refers to a linear or branched alkoxy having 1 to 6 carbon atoms, such as methoxyl, ethoxyl, propoxyl, isopropoxyl, butoxyl, isobutoxyl, sec-butoxyl, tert-butoxyl, pentoxyl, hexyloxyl, or the like.
As used herein, the term “C6-C12 benzoalicyclic group” refers to a group having 6-12 carbon atoms, and comprises indanyl, tetrahydronaphthyl, dihydronaphthyl, or the like.
As used herein, the term “C3-C7 cycloalkyl” refers to a cycloalkyl having 3-7 carbon atoms, and comprises monocyclic, bicyclic or polycyclic ring, such as cyclopropyl, cyclobutyl, methylcyclobutyl, cyclopentyl, cycloheptyl, or the like.
As used herein, the term “C2-C6 ester group” refers to a group having C1-C5 alkyl-COO— structure or a group having —COO—C1-C5 alkyl structure, wherein the alkyl can be linear or branched chain, such as CH3COO—, C2H5COO—, C3H8COO—, (CH3)2CHCOO—, —COOCH3, —COOC2H5, —COOC3H8, or the like.
As used herein, the term “C2-C4 amide group” refers to a group having C1-C3 alkyl-CO—NH— structure or a group having —CO—NH—C1-C3 alkyl structure, wherein the alkyl can be linear or branched, such as CH3—CO—NH—, C2H5—CO—NH—, C3H8—CO—NH—, —COOCH3, —CO—NH—C2H5, —CO—NH—C3H8, or the like.
As used herein, the term “C2-C4 acyl” refers to a group having C1-C5 alkyl-CO— structure, wherein the alkyl can be linear or branched, such as CH3—CO—, C2H5—CO—, C3H8—CO—, or the like.
As used herein, the term “C3-C7 heterocycloalkyl” refers to a monocyclic and polycyclic heterocycle (preferably monocyclic heterocycle) having 3-7 ring carbon atoms and 1-3 heteroatoms (preferably containing one nitrogen atom, which is the nitrogen atom commonly adjacent to R1 and R2), such as piperidinyl, tetrahydropyrrolyl, or the like.
As used herein, the term “5-7 membered carbocyclic ring” refers to any stable 5-, 6- or 7-membered monocyclic, bicyclic or polycyclic ring. The carbocyclic ring can be a saturated, partially unsaturated, or unsaturated ring, but cannot be an aromatic ring. Examples of carbocyclic ring comprise, but are not limited to, cyclopropyl, cyclobutyl, cyclobutenyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, cycloheptenyl, adamantyl, cyclooctyl, cyclooctenyl, cyclooctadienyl, bicyclo[3.3.0]octanyl, bicyclo[4.3.0]nonanyl, bicyclo[4.4.0]decanyl, bicyclo[2.2.2]octanyl, fluorenyl, indanyl.
As used herein, the term “heterocyclic ring” refers to any stable monocyclic, bicyclic or polycyclic ring, for example, 5-, 6- or 7 membered ring, wherein the heterocyclic ring contains one or more (such as 1-3) heteroatom selected from N, O and S, the heterocyclic ring can be a saturated, partially unsaturated, or unsaturated ring, but can not be an aromatic ring.
As used herein, the terms “C1-C6 haloalkyl” and “C1-C3 haloalkyl” mean that one or more hydrogen atoms of a linear or branched alkyl having 1-6 and 1-3 carbon atoms are substituted by halogen, such as monochloromethanyl, dichloroethanyl, trichloropropanyl, or the like.
As used herein, the term “C1-C4 carboxyl” refers to C1-C3 alkyl-COOH, wherein the alkyl can be linear or branched, such as CH3COOH, C2H5COOH, C3H8COOH, (CH3)2CHCOOH, or the like.
As used herein, the term “C6-C12 aryl” refers to a monocyclic or bicyclic aromatic hydrocarbon group having 6 to 12 carbon atoms in the ring, such as phenyl, naphthyl, biphenyl, or the like.
As used herein, the term “heteroaryl” refers to an optionally substituted aromatic group (for example, 5- to 7-membered monocyclic ring) which contains at least one heteroatom and at least one carbon atom, for example pyrrolyl, thienyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, furanyl, imidazolyl, thiazolyl, oxazolyl, triazolyl or the like.
As used herein, the term “halogen” refers to F, Cl, Br, and I.
As used herein, the term “substituted” means that a hydrogen atom on the group is replaced by a non-hydrogen atom group, but the valence requirement must be met and the substituted compound is chemically stable. In the specification, it should be understood that each substituent is unsubstituted, unless it is expressly described as “substituted” herein.
As used herein,
have the same meaning, and both represent unsubstituted heteroaryl or heteroaryl substituted by 1 to 5 (preferably 1 to 3) R3.
Similarly, it should be understood that substituents can be connected to a parent group or a substrate on any atom in present invention, unless the connection violates the valence requirement; and the hydrogen atoms of parent group or substrate can be on the same atom or different atoms.
As used herein, as for a numerical range from P1 to P2, the range contains not only the endpoints P1 and P2, but also any numerical points between the endpoints P1 and P2. In addition, when both P1 and P2 are positive numbers, for an integer n, its value range contains any integer value point between the endpoints P1 and P2. For example, for an integer n, when its value range is 1-10, it contains 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10; the value range 3-7 contains 3, 4, 5, 6, and 7. Typically, as for a group, C3-C7 contains C3, C4, C5, C6 and C7.
As used herein, the terms “compound of present invention”, “3-aryloxy-3-aryl-propylamine compound of present invention” and “compound of formula I” are used interchangeably, and refer to a compound of formula I, or a pharmaceutically acceptable salt, or a prodrug thereof. It should be understood that the term also comprises a mixture of the above components.
The compound of present invention not only has inhibitory effect on TRPA1, but also has certain inhibitory effect on other members of TRP family.
The term “pharmaceutically acceptable salt” refers to a salt formed by a compound of the present invention and an acid or a base suitable for use as a medicine. Pharmaceutically acceptable salts include inorganic salts and organic salts. A preferred type of salt is the salt formed by the compound of the present invention and an acid. Acids suitable for salt formation include (but are not limited to): inorganic acid such as hydrochloric acid, hydrobromic acid, hydrofluoric acid, sulfuric acid, nitric acid, phosphoric acid and the like; organic acid such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tartaric acid, citric acid, picric acid, methanesulfonic acid, toluenesulfonic acid, benzenesulfonic acid and the like; and acidic amino acid such as aspartic acid and glutamic acid. A preferred type of salt is a metal salt formed by the compound of the present invention and a base. Suitable bases for salt formation include (but are not limited to): inorganic base such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium bicarbonate, sodium phosphate and the like; and organic base such as ammonia, triethylamine, diethylamine and the like.
The preferred compounds of present invention comprise any compound selected from Table 1:
The present invention further provides a method for preparing 3-aryloxy-3-aryl-propylamine compounds of formula IA to IF.
The present invention further provides a method for preparing intermediates of formula II-III which are useful for preparing the above-mentioned compounds.
The specific synthesis method are as follows:
Synthesis of Compounds of Formula IA and IB:
Potassium tert-butoxide is added into dimethyl sulfoxide (DMSO) solution of (S)-3-(methylamino)-1-(thiophen-2-yl)-1-propanol, and the mixture is stirred for 10-20 minutes.—Quinoline or isoquinoline substituted by fluorine at different position is added, and the reaction is carried out at 80-120° C. overnight. After the reaction is completed, water is added into the reaction system, then reaction system is extracted three times with ethyl acetate, washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue is separated by column chromatography to obtain compounds of formula IA and IB.
Synthesis of Compound of Formula Ic:
wherein, A, X, Y, R1, R2, R3 and “*” are as defined above.
1) C6-C12 bicyclic heteroaryl phenol or phenol containing aliphatic ring, 1-(R3-5-membered heteroaryl)-3-chloro-propanol and triphenylphosphine (PPh3) are dissolved in anhydrous tetrahydrofuran (THF), and diisopropyl azodicarboxylate is slowly added dropwise into the system in ice bath. After the dropwise addition is completed, the reaction is carried out at 20-25° C. overnight. After the reaction is completed, the system is directly spin-dried, and the residue is separated and purified by column chromatography to afford an intermediate of formula II.
2) The intermediate of formula II is dissolved in saturated sodium iodide acetone solution, and the reaction is carried out at 50-70° C. overnight. After the reaction is completed, the solvent is spin-dried, and water is added into the system. The mixture is extracted three times with ethyl acetate, washed with saturated brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The residue is dissolved in tetrahydrofuran solution, and 40% methylamine aqueous solution is added, the reaction is carried out at 20-25° C. overnight. After the reaction is completed, the solvent was spin-dried, sodium hydroxide aqueous solution is added into the system; and the mixture is extracted three times with ethyl acetate, washed with saturated brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The residue is separated by column chromatography to afford compound I.
3) The intermediate of formula II, potassium phthalimide and sodium iodide are dissolved in N,N-dimethylformamide, and the mixture is reacted at 70-90° C. overnight. After the reaction is completed, water is added into the system, and the mixture is extracted three times with ethyl acetate, washed with water and saturated brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The residue is separated by column chromatography to afford an intermediate of formula III.
4) The intermediate of formula III is dissolved in methanol solution, hydrazine hydrate is added, and the mixture is reacted at 20-25° C. overnight. After the reaction is completed, the solvent is spin-dried, and the residue is separated by column chromatography to afford compound I.
5) Acetic acid, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 4-dimethylaminopyridine and triethylamine are dissolved in anhydrous dichloromethane solution, the mixture is stirred at room temperature for one hour, the compound of formula IC-23 in dichloromethane solution is added into the system, and the mixture is reacted at room temperature overnight. After the reaction is completed, water is added into the system, and the mixture is extracted three times with ethyl acetate, washed with water and saturated brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The residue is separated by column chromatography to afford an intermediate of formula ID.
6) The intermediate of formula II, L-proline methyl ester hydrochloride, potassium carbonate and sodium iodide are dissolved in acetonitrile solution, and the reaction is carried out at 60-80° C. overnight under nitrogen protection. After the reaction is completed, water is added into the system, and the mixture is extracted three times with ethyl acetate, washed with water and saturated brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The residue is separated by column chromatography to afford an intermediate of formula IE.
7) Compound IE and sodium hydroxide are dissolved in a mixed solution of water and tetrahydrofuran, the reaction is carried out at 30-50° C. overnight. After the reaction is completed, water is added into the system, the mixture is adjusted to pH=6-8 with diluted hydrochloric acid, extracted three times with ethyl acetate, washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford compound IF.
Synthesis of Compound Salt
The compound of formula in present invention can be converted into its pharmaceutically acceptable salt by conventional methods. For example, a solution of corresponding acid can be added into the solution of above compounds, and the solvent is removed under reduced pressure after the salt is formed, thereby forming the corresponding salt of the compound of present invention.
Transient Receptor Potential Channel Protein (TRP)
Transient receptor potential channel protein is a protein superfamily composed of important cation channels on the cell membrane. Transient receptor potential channel protein comprises multiple subfamily, such as TRPA, TRPC, TRPM, TRPV, TRPML and TRPP subfamily.
Studies have found that TRPA1 channel protein is related to a disease such as pain, epilepsy, inflammation, respiratory disorder, pruritus, urinary tract disorder, inflammatory bowel disease, etc. TRPA1 is a target useful for treating a disease such as pain, epilepsy, inflammation, respiratory disorder, pruritus, urinary tract disorder and inflammatory bowel diseases, etc.
Uses
The present invention further provides a method for inhibiting transient receptor potential channel protein (TPR), and a method for treating a disease related to transient receptor potential channel protein.
The compound of formula I of present invention can inhibit transient receptor potential channel protein, thereby preventing or treating a disease related to transient receptor potential channel protein.
In the present invention, examples of the disease related to transient receptor potential channel protein comprise (but are not limited to): pain, epilepsy, inflammation, respiratory disorder, pruritus, urinary tract disorder, and inflammatory bowel disease. Representatively, the pain comprises (but is not limited to): acute inflammatory pain, chronic inflammatory pain, visceral pain, neurogenic pain, fibromyalgia, headache (such as migraine, muscle tension pain, etc.), neuralgia (such as trigeminal neuralgia, diabetic pain, post-zoster neuralgia, etc.), or pain caused by cancer.
In a preferred embodiment, the present invention provides a method for non-therapeutically inhibiting the activity of transient receptor potential channel protein in vitro, which comprises, e.g., in an in vitro culture system, contacting a transient receptor potential channel protein or a cell expressing the protein with the compound of formula I, or a pharmaceutically acceptable salt, or a prodrug thereof in present invention, thereby inhibiting the activity of transient receptor potential channel protein.
The present invention provides a method for inhibiting transient receptor potential channel protein, which is therapeutic or non-therapeutic. Generally, the method comprises administering the compound of formula I, or a pharmaceutically acceptable salt, or a prodrug thereof in present invention to a subject in need of.
Preferably, the subject comprises human and non-human mammals (rodent, rabbit, monkey, livestock, dog, cat, and the like).
Pharmaceutical Composition and Administration Method
The invention provides a composition for inhibiting activity of transient receptor potential channel protein. The composition comprises (but is not limited to): pharmaceutical composition, food composition, dietary supplement, beverage composition, etc.
Typically, the composition is a pharmaceutical composition which comprises the compound of formula I, or a pharmaceutically acceptable salt thereof in present invention; and a pharmaceutically acceptable carrier.
In the present invention, the dosage form of pharmaceutical composition comprises (but is not limited to) oral preparation, injection and external preparation.
Representatively, the dosage form comprises (but is not limited to): tablet, injection, infusion, ointment, gel, solution, microsphere, and film.
The term “pharmaceutically acceptable carrier” refers to one or more compatible solid, semi-solid, liquid or gel fillers, which are suitable for use in humans or animals and must have sufficient purity and sufficient low toxicity. The “compatible” means each ingredient of the pharmaceutical composition and active ingredient of the drug can be blended with each other without significantly reducing the efficacy.
It should be understood that the carrier is not particularly limited. In the present invention, the carrier can be selected from materials commonly used in the art, or can be obtained by a conventional method, or is commercially available. Some examples of pharmaceutically acceptable carriers are cellulose and its derivatives (such as methylcellulose, ethylcellulose, hydroxypropylmethylcellulose, sodium carboxymethylcellulose, etc.), gelatin, talc, solid lubricants (such as stearic acid, magnesium stearate), calcium sulfate, plant oil (such as soybean oil, sesame oil, peanut oil, olive oil, etc.), polyols (such as propylene glycol, glycerin, mannitol, sorbitol, etc.), emulsifier (such as Tween), wetting agent (such as sodium lauryl sulfate), buffer agent, chelating agent, thickener, pH regulator, transdermal enhancer, colorant, flavoring agent, stabilizer, antioxidant, preservative, bacteriostatic agent, pyrogen-free water, etc.
Representatively, in addition to the active pharmaceutical ingredient, the liquid formulations can contain inert diluents commonly used in the art, such as water or other solvents, solubilizers and emulsifiers, for example, ethanol, isopropanol, ethyl carbonate, ethyl acetate, propylene glycol, 1,3-butanediol, dimethylformamide and oils, especially cottonseed oil, peanut oil, corn germ oil, olive oil, castor oil and sesame oil or a mixture thereof. In addition to these inert diluents, the composition can also contain adjuvants such as wetting agents, emulsifiers and suspensions and the like.
The pharmaceutical preparation should be matched with the mode of administration. The formulation of present invention can also be used together with other synergistic therapeutic agents (including before, simultaneous or after administering). When a pharmaceutical composition or preparation is administered, a safe and effective dose of drug is administered to a subject in need (e.g. human or non-human mammals). The safe and effective dose is usually at least 10 μg/kg body weight, and does not exceed about 8 mg/kg body weight in most cases, and preferably the dose is about 10 μg/kg body weight to about 1 mg/kg body weight. Of course, the route of administration, patient health and other factors, should also be taken into account to determine the specific dose, which are within the ability of the skilled physicians.
The Main Advantages of the Present Invention Include:
(b) The compounds of present invention have excellent in vivo efficacy as analgesia.
(c) The compounds of present invention have less toxicity and higher activity, so that the safety window is larger.
(d) The compounds of present invention have good druggability.
(e) The compounds of present invention have excellent pharmacokinetic properties.
(f) The compounds of present invention are suitable for oral administration.
The present invention will be further illustrated below with reference to the specific examples. It should be understood that these examples are only to illustrate the invention but not to limit the scope of the invention. The experimental methods with no specific conditions described in the following examples are generally performed under the conventional conditions, or according to the manufacturer's instructions. Unless indicated otherwise, parts and percentage are calculated by weight.
257 mg of (S)-3-(methylamino)-1-(thiophen-2-yl)propan-1-ol was dissolved in 10 ml of dimethyl sulfoxide solution, 168 mg of potassium tert-butoxide was added, the mixture was stirred at room temperature for 15 minutes, 883 mg of 8-fluoroquinoline was added, and the reaction was carried out at 90° C. overnight. After the reaction was completed, water was added into the reaction system, the mixture was extracted three times with ethyl acetate, washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was separated by column chromatography (methanol/dichloromethane=1:15) to afford 217 mg of the title compound as brown oil. Yield: 48.5%.
1H-NMR (400 MHz, CDCl3) δ 8.97 (dd, J=4.1, 1.3 Hz, 1H), 8.17-8.09 (m, 1H), 7.46-7.38 (m, 2H), 7.32 (t, J=7.9 Hz, 1H), 7.24 (d, J=4.9 Hz, 1H), 7.05 (d, J=7.6 Hz, 1H), 7.01 (d, J=3.2 Hz, 1H), 6.94-6.89 (m, 1H), 5.80 (dd, J=8.6, 4.8 Hz, 1H), 3.01 (dt, J=12.6, 6.9 Hz, 1H), 2.91 (dt, J=12.2, 6.2 Hz, 1H), 2.60 (dq, J=14.4, 6.2 Hz, 1H), 2.52 (s, 3H), 2.37-2.26 (m, 1H). MS (ESI, m/z): 298.88 (M+H)+.
Except that 8-fluoroquinoline was replaced with 6-fluoroquinoline, the other required raw materials, reagents and preparation method were the same as Example 1. 161 mg of the title compound as brown oil was obtained. Yield: 36.1%.
1H-NMR (400 MHz, CDCl3) δ 8.73 (dd, J=4.1, 1.2 Hz, 1H), 7.96 (t, J=7.5 Hz, 2H), 7.41 (dd, J=9.2, 2.6 Hz, 1H), 7.30 (dd, J=8.3, 4.2 Hz, 1H), 7.23 (d, J=5.0 Hz, 1H), 7.14 (d, J=2.6 Hz, 1H), 7.08 (d, J=3.3 Hz, 1H), 6.94 (dd, J=4.8, 3.7 Hz, 1H), 5.73 (dd, J=7.4, 5.7 Hz, 1H), 2.83-2.74 (m, 2H), 2.45 (s, 3H), 2.37 (td, J=14.0, 6.9 Hz, 1H), 2.16 (dq, J=13.7, 6.9 Hz, 1H). MS (ESI, m/z): 298.88 (M+H)+.
Except that 8-fluoroquinoline was replaced with 4-fluoroquinoline, the other required raw materials, reagents and preparation method were the same as Example 1. 157 mg of the title compound as brown oil was obtained. Yield: 30.1%.
1H-NMR (400 MHz, CDCl3) δ 8.63 (d, J=5.2 Hz, 1H), 8.09 (d, J=8.5 Hz, 1H), 8.03 (dd, J=8.6, 1.3 Hz, 1H), 7.66 (ddd, J=8.4, 6.9, 1.4 Hz, 1H), 7.47 (ddd, J=8.2, 6.8, 1.2 Hz, 1H), 7.25 (dd, J=4.8, 1.7 Hz, 1H), 6.97-6.91 (m, 2H), 6.84 (d, J=5.3 Hz, 1H), 5.09 (dd, J=7.8, 5.1 Hz, 1H), 3.50 (hept, J=6.9 Hz, 2H), 3.05 (s, 3H), 2.37-2.19 (m, 2H). MS (ESI, m/z): 298.88 (M+H)+.
Except that 8-fluoroquinoline was replaced with 5-fluoroquinoline, the other required raw materials, reagents and preparation method were the same as Example 1. 161 mg of the title compound as brown oil was obtained. Yield: 35.9%.
1H-NMR (400 MHz, CDCl3) δ 8.89 (dd, J=4.2, 1.8 Hz, 1H), 8.65 (dt, J=8.5, 1.3 Hz, 1H), 7.65 (d, J=8.5 Hz, 1H), 7.50 (t, J=8.1 Hz, 1H), 7.39 (dd, J=8.5, 4.2 Hz, 1H), 7.22 (dd, J=5.1, 1.2 Hz, 1H), 7.06 (dd, J=3.6, 1.2 Hz, 1H), 6.97-6.88 (m, 2H), 5.81 (dd, J=7.6, 5.4 Hz, 1H), 2.83 (t, J=6.4 Hz, 2H), 2.54-2.38 (m, 4H), 2.24 (dtd, J=14.0, 7.0, 5.3 Hz, 1H). MS (ESI, m/z): 298.88 (M+H)+
Except that 8-fluoroquinoline was replaced with 4-fluoroisoquinoline, the other required raw materials, reagents and preparation method were the same as Example 1. 141 mg of the title compound as brown oil was obtained. Yield: 31.5%.
1H-NMR (400 MHz, CDCl3) δ 8.84 (s, 1H), 8.27 (d, J=8.3 Hz, 1H), 8.12 (s, 1H), 7.91 (d, J=8.2 Hz, 1H), 7.71 (t, J=7.6 Hz, 1H), 7.61 (t, J=7.5 Hz, 1H), 7.22 (d, J=4.9 Hz, 1H), 7.11 (d, J=3.3 Hz, 1H), 6.95-6.88 (m, 1H), 5.94-5.86 (m, 1H), 2.96 (q, J=7.3 Hz, 1H), 2.90 (t, J=7.0 Hz, 1H), 2.55 (dd, J=14.0, 7.0 Hz, 1H), 2.50 (s, 3H), 2.32 (dd, J=13.5, 6.2 Hz, 1H). MS (ESI, m/z): 298.88 (M+H)+.
Except that 8-fluoroquinoline was replaced with 8-fluoroisoquinoline, the other required raw materials, reagents and preparation method were the same as Example 1. 152 mg of the title compound as brown oil was obtained. Yield: 33.9%.
1H-NMR (400 MHz, CDCl3) δ 9.72 (s, 1H), 8.53 (d, J=5.7 Hz, 1H), 7.56 (d, J=5.7 Hz, 1H), 7.47 (t, J=8.0 Hz, 1H), 7.33 (d, J=8.2 Hz, 1H), 7.23 (d, J=5.0 Hz, 1H), 7.09 (d, J=3.4 Hz, 1H), 6.99-6.93 (m, 2H), 5.85 (dd, J=7.5, 5.5 Hz, 1H), 2.84 (q, J=6.4, 6.0 Hz, 2H), 2.54-2.47 (m, 1H), 2.45 (s, 3H), 2.24 (dq, J=13.7, 6.9 Hz, 1H). MS (ESI, m/z): 298.88 (M+H)+.
Except that 8-fluoroquinoline was replaced with 5-fluoroisoquinoline, the other required raw materials, reagents and preparation method were the same as Example 1, 163 mg of the title compound as brown oil was obtained. Yield: 36.4%.
1H-NMR (400 MHz, CDCl3) δ 9.17 (s, 1H), 8.53 (d, J=5.9 Hz, 1H), 8.07 (d, J=5.8 Hz, 1H), 7.50 (d, J=8.2 Hz, 1H), 7.39 (t, J=8.0 Hz, 1H), 7.22 (dd, J=5.0, 1.2 Hz, 1H), 7.08-7.04 (m, 2H), 6.93 (dd, J=5.1, 3.5 Hz. 1H), 5.83 (dd, J=7.7, 5.4 Hz, 1H), 2.90-2.84 (m, 2H), 2.55-2.44 (m, 4H), 2.30-2.25 (m, 1H). MS (ESI, m/z): 298.88 (M+H)+.
480 mg of (R)-3-chloro-1-(thiophen-2-yl)propan-1-ol, 364 mg of 7-hydroxybenzofuran and 784 mg of triphenylphosphine were dissolved in 20 ml of anhydrous tetrahydrofuran, and 589 μl of diisopropyl azodicarboxylate was slowly added dropwise into the system under ice bath condition. After the dropwise addition was completed, the system was shifted to room temperature and reacted overnight. After the reaction was completed, the system was directly spin-dried, and the residue was separated and purified by column chromatography to afford 600 mg of the title compound as colorless oil. Yield: 75.43%.
1H NMR (500 MHz, CDCl3) δ 7.61 (t, J=3.1 Hz, 1H), 7.39 (dd, J=1.7, 0.7 Hz, 1H), 7.21 (dt, J=8.2, 1.9 Hz, 1H), 7.11-7.06 (m, 1H), 6.88 (d, J=7.9 Hz, 1H), 6.76 (dd, J=8.1, 2.1 Hz, 1H), 6.33 (d, J=3.2 Hz, 1H), 6.30 (dd, J=3.3, 1.8 Hz, 1H), 5.70 (dd, J=8.4, 5.1 Hz, 1H), 3.89 (ddd, J=11.1, 8.2, 5.4 Hz, 1H), 3.73-3.65 (m, 1H), 2.80-2.70 (m, 1H), 2.51-2.42 (m, 1H). MS (ESI, m/z): 293 (M+H)+.
600 mg of Intermediate II-1 was dissolved in saturated sodium iodide solution in acetone, and the mixture was refluxed overnight. After the reaction was completed, the solvent was spin-dried, water was added into the system, and the mixture was extracted three times with ethyl acetate, washed with saturated brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The residue was dissolved in 20 ml of tetrahydrofuran solution, 2 ml of 40% methylamine aqueous solution was added, and the reaction was carried out overnight. After the reaction was completed, the solvent was spin-dried, sodium hydroxide aqueous solution was added into the system, then the mixture was extracted with ethyl acetate three times, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was separated by column chromatography (methanol/dichloromethane=1:15) to afford 200 mg of the title compound as colorless oil. Yield: 33.96%.
1H NMR (400 MHz, CDCl3) δ 7.63 (d, J=2.0 Hz, 1H), 7.20 (t, J=6.6 Hz, 2H), 7.08-6.99 (m, 2H), 6.88 (dd, J=4.9, 3.6 Hz, 1H), 6.80 (d, J=7.9 Hz, 1H), 6.75 (d, J=2.0 Hz, 1H), 5.93 (dd, J=8.2, 4.4 Hz, 1H), 3.30 (t, J=7.0 Hz, 2H), 2.82-2.69 (m, 4H), 2.65-2.54 (m, 1H). MS (ESI, m/z): 287.87 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(thiophen-3-yl)prop-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 200 mg of the title compound as yellow oil was obtained. Yield: 33.9%.
1H NMR (500 MHz, CDCl3) δ 7.63 (d, J=2.1 Hz, 1H), 7.27 (dd, J=5.0, 3.0 Hz, 1H), 7.24 (d, J=2.1 Hz, 1H), 7.18-7.11 (m, 2H), 7.01 (t, J=7.9 Hz, 1H), 6.75 (d, J=2.1 Hz, 1H), 6.72 (d, J=7.8 Hz, 1H), 5.64 (dd, J=8.0, 5.0 Hz, 1H), 2.94-2.81 (m, 2H), 2.48 (s, 3H), 2.46-2.32 (m, 1H), 2.24-2.13 (in, 1H). MS (ESI, m/z): 287.76 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(furan-3-yl)prop-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 100 mg of the title compound as colorless oil was obtained. Yield: 9.89%.
1H NMR (500 MHz, CDCl3) δ 7.62 (d, J=2.1 Hz, 1H), 7.40 (s, 1H), 7.35 (t, J=1.7 Hz, 1H), 7.17 (dd, J=7.8, 0.8 Hz, 1H), 7.05 (t, J=7.9 Hz, 1H), 6.80 (d, J=7.7 Hz, 1H), 6.75 (d, J=2.1 Hz, 1H), 6.46 (d, J=1.1 Hz, 1H), 5.56 (dd, J=7.7, 5.4 Hz, 1H), 2.90-2.78 (m, 2H), 2.46 (s, 3H), 2.35 (td, J=13.9, 7.4 Hz, 1H), 2.13 (dtd, J=12.4, 7.0, 5.5 Hz, 1H). MS (ESI, m/z): 271.88 (M+H)+
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(furan-2-yl)prop-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 30 mg of the title compound as colorless oil was obtained. Yield: 3.22%.
1H NMR (500 MHz, CDCl3) δ 7.61 (d, J=2.1 Hz, 1H), 7.36 (d, J=1.1 Hz, 1H), 7.20 (d, J=7.7 Hz, 1H), 7.06 (dd, J=10.5, 5.3 Hz, 1H), 6.82 (d, J=7.7 Hz, 1H), 6.74 (dd, J=7.8, 2.1 Hz, 1H), 6.31 (d, J=3.2 Hz, 1H), 6.27 (dd, J=3.2, 1.8 Hz, 1H), 5.60 (dd, J=7.9, 5.3 Hz, 1H), 3.13-2.99 (m, 2H), 2.63-2.56 (m, 4H), 2.44 (ddd, J=14.1, 12.4, 7.0 Hz, 1H). MS (ESI, m/z): 271.88 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(5-methylthiophen-2-yl) propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 160 mg of the title compound as colorless oil was obtained. Yield: 14.24%.
1H NMR (500 MHz, CDCl3) δ 7.62 (d, J=2.1 Hz, 1H), 7.17 (dd, J=7.8, 0.8 Hz, 1H), 7.04 (t, J=7.9 Hz, 1H), 6.82 (d, J=7.6 Hz, 1H), 6.79 (d, J=3.4 Hz, 1H), 6.74 (dd, J=6.6, 2.2 Hz, 1H), 6.58-6.51 (m, 1H), 5.71 (dd, J=7.8, 5.5 Hz, 1H), 2.93-2.81 (m, 2H), 2.47 (s, 3H), 2.45-2.38 (m, 4H), 2.25-2.16 (m, 1H). MS (ESI, m/z): 301.87 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(5-chlorothiophene-2-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 300 mg of the title compound as colorless oil was obtained. Yield: 20.84%.
1H NMR (500 MHz, CDCl3) δ 7.63 (d, J=2.1 Hz, 1H), 7.20 (d, J=7.8 Hz, 1H), 7.05 (t, J=7.9 Hz, 1H), 6.80 (dd, J=12.0, 5.7 Hz, 2H), 6.75 (t, J=4.6 Hz, 1H), 6.70 (d, J=3.8 Hz, 1H), 5.75 (dd, J=8.1, 5.2 Hz, 1H), 3.04-2.89 (m, 2H), 2.57-2.43 (m, 4H), 2.27 (ddd, J=13.7, 12.0, 6.7 Hz, 1H). MS (ESI, m/z): 321.78 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with 3-chloro-1-(thiazol-2-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. After racemate of compound IC-7 was obtained, 60 mg of the title compound as yellow oil was obtained by chiral resolution. Yield: 6.72%.
1H NMR (500 MHz, CDCl3) δ 7.76 (d, J=3.2 Hz, 1H), 7.64 (d, J=2.1 Hz, 1H), 7.33 (d, J=3.2 Hz, 1H), 7.25 (d, J=0.9 Hz, 1H), 7.08 (t, J=7.9 Hz, 1H), 6.89 (d, J=7.3 Hz, 1H), 6.78 (d, J=2.2 Hz, 1H), 6.05 (t, J=6.0 Hz, 1H), 3.33 (t, J=6.9 Hz, 2H), 2.81-2.67 (m, 5H). MS (ESI, m/z): 288.77 (M+H)+.
Except that methylamine aqueous solution was replaced with dimethylamine, the other required raw materials, reagents and preparation method were the same as Example 9. 130 mg of the title compound as colorless oil was obtained. Yield: 34.67%.
1H NMR (400 MHz, CDCl3) δ 7.62 (d, J=2.0 Hz, 1H), 7.23 (d, J=5.0 Hz, 1H), 7.17 (d, J=7.8 Hz, 1H), 7.03 (t, J=7.9 Hz, 2H), 6.96-6.87 (m, 1H), 6.82 (d, J=7.9 Hz, 1H), 6.74 (d, J=2.1 Hz, 1H), 5.88-5.79 (m, 1H), 2.60 (t, J=6.9 Hz, 2H), 2.47 (dt, J=21.7, 7.4 Hz, 1H), 2.32 (s, 6H), 2.22 (dt, J=20.5, 6.8 Hz, 1H). MS (ESI, m/z): 301.88 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with 4-hydroxybenzofuran, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 15 mg of the title compound as yellow oil was obtained. Yield: 1.40%.
1H NMR (400 MHz, CDCl3) δ 7.53 (d, J=2.1 Hz, 1H), 7.20 (d, J=5.0 Hz, 1H), 7.14-7.07 (m, 3H), 6.92-6.87 (m, 2H), 6.72 (dd, J=6.6, 2.1 Hz, 1H), 5.87 (dd, J=7.7, 4.8 Hz, 1H), 3.34-3.19 (m, 2H), 2.78 (td, J=14.6, 7.3 Hz, 1H), 2.66 (dt, J=15.1, 6.4 Hz, 4H). MS (ESI, m/z): 287.87 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with 4-indanol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 16 mg of the title compound as brown oil was obtained. Yield: 9.9%.
1H NMR (400 MHz, CDCl3) δ 7.21 (dd, J=5.0, 1.2 Hz, 1H), 7.03-6.96 (m, 2H), 6.92 (dd, J=5.0, 3.5 Hz, 1H), 6.81 (d, J=7.3 Hz, 1H), 6.65 (d, J=8.0 Hz, 1H), 5.57 (dd, J=7.8, 5.0 Hz, 1H), 2.87 (dt, J=19.9, 7.3 Hz, 6H), 2.47 (s, 3H), 2.41-2.30 (m, 1H), 2.25-2.14 (m, 1H), 2.06 (p, J=7.0 Hz, 2H). MS (ESI, m/z): 287.87 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(thiophen-3-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Example 18. 60 mg of the title compound as brown oil was obtained. Yield: 8.6%.
1H NMR (500 MHz, CDCl3) δ 7.27 (dd, J=4.0, 2.0 Hz, 1H), 7.20-7.15 (m, 1H), 7.06 (dt, J=3.8, 1.9 Hz, 1H), 6.96 (t, J=7.9 Hz, 1H), 6.80 (d, J=7.6 Hz, 1H), 6.54 (d, J=8.2 Hz, 1H), 5.40 (dd, J=7.9, 4.7 Hz, 1H), 2.91 (dd, J=16.1, 8.4 Hz, 4H), 2.82 (ddd, J=9.8, 7.1, 3.8 Hz, 2H), 2.47 (s, 3H), 2.31-2.23 (m, 1H), 2.19-2.11 (m, 1H), 2.11-2.03 (m, 2H). MS (ESI, m/z): 287.76 (M+H).
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(furan-2-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Example 18. 10 mg of the title compound as brown oil was obtained. Yield: 4.2%.
1H NMR (500 MHz, CDCl3) δ 7.36 (dd, J=1.8, 0.8 Hz, 1H), 7.03 (dd, J=14.9, 7.1 Hz, 1H), 6.83 (d, J=7.4 Hz, 1H), 6.67 (d, J=8.1 Hz, 1H), 6.30 (dd, J=3.2, 1.8 Hz, 1H), 6.25 (d, J=3.2 Hz, 1H), 5.30 (dd, J=7.6, 5.4 Hz, 1H), 2.92-2.79 (m, 6H), 2.48 (s, 3H), 2.35 (td, J=14.0, 7.2 Hz, 1H), 2.23 (ddd, J=14.0, 12.5, 7.1 Hz, 1H), 2.08-2.01 (m, 2H). MS (ESI, m/z): 271.88 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(furan-3-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Example 18. 13 mg of the title compound as brown oil was obtained. Yield: 4.6%.
1H NMR (500 MHz, CDCl3) δ 7.35 (d, J=1.4 Hz, 2H), 7.01 (t, J=7.8 Hz, 1H), 6.81 (d, J=7.4 Hz, 1H), 6.63 (d, J=8.1 Hz, 1H), 6.38 (t, J=1.3 Hz, 1H), 5.29 (dd, J=7.7, 5.0 Hz, 1H), 2.94-2.85 (m, 4H), 2.83-2.75 (m, 2H), 2.46 (s, 3H), 2.22 (td, J=13.9, 7.4 Hz, 1H), 2.11-2.00 (m, 3H). MS (ESI, m/z): 271.63 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-I-ol was replaced with (R)-3-chloro-1-(thiazol-3-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Example 18. After racemate of compound IC-14 was obtained, 35 mg of the title compound as yellow oil was obtained by chiral resolution. Yield: 5.9%.
1H NMR (400 MHz, CDCl3) δ 7.74 (d, J=3.2 Hz, 1H), 7.28 (d, J=3.2 Hz, 1H), 7.01 (t, J=7.8 Hz, 1H), 6.85 (d, J=7.4 Hz, 1H), 6.65 (d, J=8.1 Hz, 1H), 5.70 (dd, J=7.3, 5.2 Hz, 1H), 3.01 (d, J=7.5 Hz, 1H), 2.98-2.82 (m, 5H), 2.48 (s, 3H), 2.44-2.24 (m, 2H), 2.14-2.02 (m, 2H). MS (ESI, m/z): 288.87 (M+H)+
Except that methylamine aqueous solution was replaced with dimethylamine, the other required raw materials, reagents and preparation method were the same as Example 18. 21 mg of the title compound as brown oil was obtained. Yield: 10.1%.
1H NMR (400 MHz, CDCl3) δ 7.22 (dd, J=5.0, 1.2 Hz, 1H), 7.00 (dd, J=10.5, 5.2 Hz, 2H), 6.93 (dd, J=5.0, 3.5 Hz, 1H), 6.82 (d, J=7.5 Hz, 1H), 6.65 (d, J=8.1 Hz, 1H), 5.57 (dd, J=7.6, 5.3 Hz, 1H), 2.90 (dt, J=20.0, 6.5 Hz, 4H), 2.76 (s, 2H), 2.57-2.36 (m, 7H), 2.30 (s, 1H), 2.13-1.98 (m, 2H). MS (ESI, m/z): 301.77 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with 5-indanol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 15 mg of the title compound as yellow oil was obtained. Yield: 9.7%.
1H NMR (400 MHz, CDCl3) δ 7.21 (dd, J=5.0, 1.1 Hz, 1H), 7.06-6.98 (m, 2H), 6.91 (dd, J=5.0, 3.5 Hz, 1H), 6.78 (s, 1H), 6.68 (d, J=8.6 Hz, 1H), 5.56 (dd, J=7.8, 4.6 Hz, 1H), 3.08 (t, J=7.3 Hz, 2H), 2.79 (dt, J=12.2, 7.4 Hz, 4H), 2.61 (s, 3H), 2.03 (q, J=7.6 Hz, 4H). MS (ESI, m/z): 287.88 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with tetrahydronaphthol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 30 mg of the title compound as yellow oil was obtained. Yield: 13.6%.
1H NMR (400 MHz, CDCl3) δ 7.19-7.14 (m, 1H), 6.98-6.93 (m, 2H), 6.67 (d, J=7.9 Hz, 1H), 6.53 (d, J=8.0 Hz, 1H), 4.82 (dd, J=12.5, 3.4 Hz, 1H), 2.83-2.64 (m, 5H), 2.56-2.31 (m, 5H), 2.12 (m, 1H), 1.84-1.66 (m, 4H). MS (ESI, m/z): 301.77 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with 5,8-dihydronaphthol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 65 mg of the title compound as brown oil was obtained. Yield: 25.3%.
1H NMR (400 MHz, DMSO) δ 9.31 (s, 1H), 7.32 (dd, J=5.1, 1.2 Hz, 1H), 7.02 (d, J=8.4 Hz, 1H), 6.93 (dd, J=5.1, 3.5 Hz, 1H), 6.88 (d, J=3.1 Hz, 1H), 6.70 (d, J=8.3 Hz, 1H), 5.85 (dd, J=22.1, 10.2 Hz, 2H), 4.38 (t, J=7.6 Hz, 1H), 3.42 (s, 1H), 3.15 (d, J=10.1 Hz, 4H), 2.91-2.68 (m, 3H), 2.57-2.52 (m, 3H), 2.30-2.20 (m, 2H). MS (ESI, m/z): 299.76 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with 4-hydroxy-2-methylisoindoline-1,3-dione, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 163 mg of the title compound as brown oil was obtained. Yield: 36.4%.
1H NMR (400 MHz, CDCl3) 7.52 (t, J=7.8 Hz, 1H), 7.43 (d, 1=7.3 Hz, 1H), 7.28 (d, J=4.9 Hz, 1H), 7.04 (dd, J=11.3, 5.6 Hz, 2H), 6.97 (dd, J=4.9, 3.4 Hz, 1H), 6.05 (s, 1H), 3.34 (s, 2H), 3.14 (s, 3H), 3.02 (s, 1H), 2.88 (s, 3H), 2.43 (d, J=15.0 Hz, 1H). MS (ESI, m/z): 330.76 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with 8-hydroxyimidazo[1,2-a]pyridine, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 43 mg of the title compound as brown oil was obtained. Yield: 11.7%.
1H NMR (400 MHz, CDCl3) δ 7.95 (d, J=6.4 Hz, 1H), 7.64 (s, 1H), 7.53 (d, J=11.9 Hz, 1H), 7.35-7.28 (m, 1H), 6.91 (d, J=3.4 Hz, 2H), 6.69 (t, J=7.1 Hz, 1H), 6.62 (d, J=7.2 Hz, 1H), 5.85 (dd, J=11.5, 2.7 Hz, 1H), 3.55 (t, J=10.1 Hz, 1H), 3.34-3.24 (m, 1H), 2.85 (s, 3H), 2.78 (dd, J=11.1, 3.3 Hz, 1H), 2.64-2.52 (m, 1H). MS (ESI, m/z): 287.77 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with 4-hydroxy-1H-benzo[d]imidazole-2(3H)-one, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 43 mg of the title compound as brown oil was obtained. Yield: 9.4%.
1H NMR (400 MHz, CD3OD) δ 7.35 (dd, J=5.1, 1.1 Hz, 1H), 7.11 (d, J=2.8 Hz, 1H), 6.95 (dd, J=5.1, 3.5 Hz, 1H), 6.88-6.81 (m, 1H), 6.67 (dd, J=8.1, 2.8 Hz, 2H), 5.77 (dd, J=8.1, 4.8 Hz, 1H), 3.11-2.98 (m, 2H), 2.60 (s, 3H), 2.50-2.39 (m, 1H), 2.32-2.23 (m, 1H). MS (ESI, 303.88 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with 5-fluoroquinoxaline, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 230 mg of the title compound as brown oil was obtained. Yield: 40.5%.
1H NMR (400 MHz, CDCl3) δ 8.98 (d, J=11.6 Hz, 2H), 7.83 (d, J=8.5 Hz, 1H), 7.58 (t, J=8.1 Hz, 1H), 7.35 (d, J=4.7 Hz, 1H), 7.05-6.95 (m, 3H), 5.67 (d, J=6.1 Hz, 1H), 3.45 (s, 2H), 2.93 (s, 3H), 2.76 (s, 1H), 2.64 (s, 1H). MS (ESI, m/z): 299.88 (M+H)+.
160 mg of Intermediate II-1, 303 mg of potassium phthalimide and 25 mg of sodium iodide were dissolved in 5 ml of N,N-dimethylformamide, and the reaction was carried out at 90° C. under nitrogen protection overnight. After the reaction was completed, water was added into the system, and the mixture was extracted three times with ethyl acetate, washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was separated by column chromatography (ethyl acetate/petroleum ether=1:5) to afford 140 mg of the title compound as yellow solid. Yield: 63.49%.
NMR (500 MHz, CDCl3) δ 7.81-7.78 (m, 2H). 7.68 (dd, J=5.5, 3.0 Hz, 2H), 7.45 (d, J=2.1 Hz, 1H), 7.18 (dd, J=5.0, 1.1 Hz, 1H), 7.14 (dd, J=7.8, 0.8 Hz, 1H), 7.06 (d, J=3.0 Hz, 1H), 7.04-6.97 (m, 1H), 6.86 (dt, J=10.3, 5.2 Hz, 1H), 6.78 (d, J=7.4 Hz, 1H), 6.68 (d, J=2.1 Hz, 1H), 5.82 (dd, J=7.8, 5.2 Hz, 1H), 4.07-3.89 (m, 2H), 2.66 (td, J=14.4, 7.3 Hz, 1H), 2.47-2.36 (m, 1H). MS (ESI, m/z): 404 (M+H)+.
140 mg of Intermediate III-1 and 87 mg of hydrazine hydrate were dissolved in 5 ml of methanol solution, and the reaction was carried out at room temperature overnight. After the reaction was completed, the solvent was spin-dried, and the residue was separated by column chromatography (methanol/dichloromethane=1:15) to afford 30 mg of the title compound as colorless oil. Yield: 31.63%.
1H NMR (500 MHz, DMSO) δ 7.97 (d, J=2.1 Hz, 1H), 7.49 (dd, J=5.0, 1.1 Hz, 1H), 7.24-7.17 (m, 2H), 7.11-7.03 (m, 1H), 6.99 (dd, J=5.0, 3.5 Hz, 1H), 6.95 (d, J=7.5 Hz, 1H), 6.93 (d, J=2.1 Hz, 1H), 6.04 (dd, J=7.8, 5.5 Hz, 1H), 2.99-2.86 (m, 2H), 2.44-2.35 (m, 1H), 2.21 (ddt, J=11.5, 9.3, 5.8 Hz, 1H). MS (ESI, m/z): 273.77 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(furan-3-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8, and 31-32. 90 mg of the title compound as colorless oil was obtained. Yield: 12.71%.
1H NMR (500 MHz, CDCl3) δ 7.62 (d, J=2.1 Hz, 1H), 7.42-7.37 (m, 1H), 7.35 (t, J=1.7 Hz, 1H), 7.18 (dd, J=7.8, 0.9 Hz, 1H), 7.08-7.01 (m, 1H), 6.79 (dd, J=7.9, 0.7 Hz, 1H), 6.75 (d, J=2.2 Hz, 1H), 6.45 (dd, J=1.7, 0.7 Hz, 1H), 5.57 (dd, J=8.1, 5.0 Hz, 1H), 3.03-2.91 (m, 2H), 2.31 (ddt, J=14.1, 8.1, 6.4 Hz, 1H), 2.06 (dtd, J=9.4, 7.1, 5.1 Hz, 1H). MS (ESI, m/z): 257.77 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(furan-2-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8, and 31-32. 85 mg of the title compound as colorless oil was obtained. Yield: 16.53%.
1H NMR (500 MHz, CDCl3) δ 7.62 (d, J=2.1 Hz, 1H), 7.37 (dd, J=1.6, 1.0 Hz, 1H), 7.20 (dd, J=7.8, 0.9 Hz, 1H), 7.06 (t, J=7.9 Hz, 1H), 6.87-6.80 (m, 1H), 6.75 (d, J=2.1 Hz, 1H), 6.33-6.24 (m, 2H), 5.59 (dd, J=8.0, 5.5 Hz, 1H), 3.09-2.93 (m, 2H), 2.43 (dq, J=7.9, 6.4 Hz, 1H), 2.22 (qd, J=12.5, 6.9 Hz, 1H). MS (ESI, m/z): 257.64 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(thiophen-3-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8 and 31-32. 60 mg of the title compound as colorless oil was obtained. Yield: 14.56%.
1H NMR (500 MHz, CDCl3) δ 7.62 (d, J=1.9 Hz, 1H), 7.25-7.22 (m, 2H), 7.13 (t, J=7.4 Hz, 1H), 7.09 (d, J=4.6 Hz, 1H), 6.97 (t. J=7.9 Hz, 1H). 6.71 (d, J=2.0 Hz, 1H), 6.67 (d, J=8.0 Hz, 1H), 5.65 (dd, J=7.9, 4.2 Hz, 1H), 3.30-3.11 (m, 2H), 2.49 (dd, J=14.1, 7.4 Hz, 1H), 2.34 (dd, J=12.9, 5.8 Hz, 1H). MS (ESI, m/z): 273.77 (M+H)+.
Except that 7-hydroxybenzofuran was replaced with benzo[b]thiophen-5-ol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 20 mg of the title compound as yellow oil was obtained. Yield: 3.30%.
1H NMR (500 MHz, CDCl3) δ 7.68 (d, J=8.8 Hz, 1H), 7.39 (d, J=5.4 Hz, 1H), 7.31 (d, J=2.4 Hz, 1H), 7.22 (dd, J=5.0, 1.1 Hz, 1H), 7.18 (d, J=5.4 Hz, 1H), 7.04-6.99 (m, 2H), 6.92 (dd, J=5.0, 3.5 Hz, 1H), 5.63 (dd, J=7.7, 5.2 Hz, 1H), 2.93-2.81 (m, 2H), 2.49 (s, 3H), 2.39 (tt, J=12.5, 6.3 Hz, 1H), 2.22 (ddd, J=14.0, 12.4, 7.0 Hz, 1H). MS (ESI, m/z): 303.76 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(furan-3-yl)propan-1-ol, the other required raw materials, reagents and preparation method were the same as Example 17. 40 mg of the title compound as colorless oil was obtained. Yield: 5.08%.
1H NMR (500 MHz, CDCl3) δ 7.52 (dd, J=10.8, 2.2 Hz, 1H), 7.41 (d, J=0.7 Hz, 1H), 7.35 (t, J=1.7 Hz, 1H), 7.15-7.07 (m, 2H), 6.87 (d, J=2.1 Hz, 1H), 6.70-6.64 (m, 1H), 6.44-6.39 (m, 1H), 5.49 (dd, J=7.6, 5.0 Hz, 1H), 2.95 (t, J=7.2 Hz, 2H), 2.53 (s, 3H), 2.42 (td, J=14.3, 7.5 Hz, 1H), 2.30-2.23 (m, 1H). MS (ESI, m/z): 271.75 (M+H)+.
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-(oxazol-5-yl)propyl-1-ol, the other required raw materials, reagents and preparation method were the same as Examples 8-9. 63 mg of the title compound as yellow oil was obtained. Yield: 21%.
1H NMR (500 MHz, CDCl3) δ 7.83 (s, 1H), 7.62 (d, J=2.1 Hz, 1H), 7.23 (dd, J=7.8, 0.9 Hz, 1H), 7.08 (dd, J=10.4, 5.3 Hz, 1H), 7.03 (s, 1H), 6.87-6.81 (m, 1H), 6.76 (d, J=2.2 Hz, 1H), 5.74 (dd, J=8.0, 5.4 Hz, 1H), 3.00-2.87 (m, 2H), 2.53-2.49 (m, 4H), 2.36-2.26 (m, 1H). MS (ESI, m/z): 272.76 (M+H)+.
19 mg of acetic acid, 59 mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 38 mg of 4-dimethylaminopyridine and 52 mg of triethylamine were dissolved in 5 ml anhydrous dichloromethane, the mixture was stirred at room temperature for 1 h, 5 ml of dichloromethane solution containing 70 mg of compound Ic-23 was added into the system, and the reaction was carried out at room temperature overnight. After the reaction was completed, water was added into the system, the mixture was extracted three times with ethyl acetate, washed with saturated brine, dried with anhydrous sodium sulfate, filtered, and concentrated. The residue was separated by column chromatography (methanol/dichloromethane=1:20) to afford 18 mg of the title compound as yellow oil. Yield: 22.29%.
1H NMR (500 MHz, CDCl3) δ 7.64 (dd, J=9.8, 2.2 Hz, 1H), 7.24 (dd, J=5.0, 1.1 Hz, 1H), 7.21 (dd, J=7.8, 0.9 Hz, 1H), 7.07-7.02 (m, 1H), 7.01-6.98 (m, 1H), 6.96-6.91 (m, 1H), 6.78 (d, J=2.2 Hz, 1H), 6.75 (d, J=7.9 Hz, 1H), 6.31 (s, 1H), 5.78-5.70 (m, 1H), 3.69-3.59 (m, 1H), 3.55-3.44 (m, 1H), 2.42-2.24 (m, 2H), 1.99 (s, 3H). MS (ESI, m/z): 315.89 (M+H)+.
100 mg of Intermediate II-1, 113 mg of methyl L-proline ester hydrochloride, 283 mg of potassium carbonate and 10 mg of sodium iodide were dissolved in 5 ml of acetonitrile, and the reaction was carried out at 75° C. overnight under nitrogen protection. After the reaction was completed, water was added into the system, the mixture was extracted with ethyl acetate three times, washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was separated by column chromatography (ethyl acetate/petroleum ether=1:5) to afford 16 mg of the title compound as colorless oil. Yield: 12.15%.
1H NMR (500 MHz, CDCl3) δ 7.62 (d, J=2.1 Hz, 1H), 7.23-7.19 (m, 1H), 7.16 (dd, J=7.0, 5.7 Hz, 1H), 7.03 (ddd, J=7.8, 6.0, 1.5 Hz, 2H), 6.93-6.89 (m, 1H), 6.83 (t, J=8.9 Hz, 1H), 6.74 (t, J=2.1 Hz, 1H), 5.84 (dd, J=15.6, 7.6 Hz, 1H), 3.47 (s, 2H), 3.21 (s, 2H), 2.94 (d, J=53.0 Hz, 1H), 2.66 (s, 1H), 2.44 (s, 2H), 2.15 (d, J=49.5 Hz, 2H), 1.95 (s, 2H), 1.83 (s, 1H). MS (ESI, m/z): 386.13 (M+H)+
100 mg of compound IE and 50 mg of sodium hydroxide were dissolved in 15 ml mixed solution of water and tetrahydrofuran, and the reaction was carried out at 40° C. overnight. After the reaction was completed, water was added into the system, and the reaction system was adjusted to pH=7 with diluted hydrochloric acid, extracted with ethyl acetate three times, washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to afford 33.7 mg of the title compound as colorless oil. Yield: 35%.
1H NMR (500 MHz, DMSO) δ 7.96 (d, J=2.0 Hz, 1H), 7.47 (d, J=4.9 Hz, 1H), 7.19 (t, J=6.1 Hz, 2H), 7.06 (td, J=7.8, 2.8 Hz, 1H), 6.94 (ddd, J=9.9, 6.4, 2.9 Hz, 3H), 5.98 (dd, J=12.9, 7.5 Hz, 1H), 3.45-3.42 (m, 1H), 3.09 (ddd, J=20.6, 10.9, 5.1 Hz, 2H), 2.92 (s, 1H), 2.82-2.68 (m, 1H), 2.44-2.34 (m, 1H), 2.26-2.08 (m, 2H), 1.94-1.77 (m, 2H), 1.70 (dd, J=18.3, 10.6 Hz, 1H). MS (ESI, m/z): 371.94 (M+H)+.
Preparation of Compound of Formula C1 was Briefly Described as Follows:
Except that (R)-3-chloro-1-(thiophen-2-yl)propyl-1-ol was replaced with (R)-3-chloro-1-phenylpropane-1-ol, the other required raw materials, reagents and preparation method were the same as Example 18. 14 mg of compound C1 was obtained. Yield: 18%.
1H NMR (400 MHz, CDCl3) δ 7.46-7.14 (m, 5H), 6.90 (t, J=7.7 Hz, 1H), 6.77 (d, J=7.4 Hz, 1H), 6.41 (d, J=8.1 Hz, 1H), 5.33 (dd, J=8.0, 4.4 Hz, 1H), 3.13 (dd, J=13.5, 6.0 Hz, 2H), 2.91 (dt, J=12.3, 7.5 Hz, 4H), 2.62 (s, 3H), 2.52-2.36 (m, 2H), 2.13-2.00 (m, 2H). MS (ESI, m/z): 282.20 (M+H)+.
TRPA1 Inhibitory Activity
The inhibitory activity of some compounds in the Examples of present invention on transient receptor potential channel protein TRPA1 was tested in this example. The compound of formula A (WO2010075353) was used as a positive control compound:
The method was as below:
IonWorks Barracuda (IWB) automated patch clamp detection was used as test method: HEK293 cells stably expressing TRPA1 were placed in DMEM medium containing 15 μg/mL Blasticidin S HCl, 200 μg/mL Hygromycin B and 10% FBS in the T175 culture flask, and cultured in 37° C., 5% CO2 incubator. When the cell density reached about 80%, the culture medium was removed, rinsed with phosphate buffered saline (PBS) without calcium and magnesium. 3 mL of Trypsin was added to digest for 2 min, 7 mL of culture medium was added to terminate the digestion. The cells were collected to 15 mL centrifuge tube and centrifuged at 800 rpm for 3 min. After the supernatant was removed, the cells were added to appropriate volume of extracellular fluid for re-suspending, and the cell density was controlled at 2-3×106/mL for IWB experiment. Extracellular fluid formulation (in mM): 140 NaCl, 5 KCl, 1 MgCl2, 10 HEPES, 0.5 EGTA, 10 Glucose (pH 7.4); intracellular fluid formulation (in mM): 140 CsCl, 10 HEPES, 5 EGTA, 0.1 CaCl2, 1 MgCl2 (pH 7.2). 28 mg/mL of amphotericin B was freshly prepared with DMSO on the day of experiment, and then final concentration of 0.1 mg/mL was prepared with intracellular fluid.
Population patch clamp (PPC) plate was used in IWB experiment. The entire detection process was automatically carried out by the instrument. Extracellular fluid was added into 384 wells of PPC plate, and 6 L of the intracellular fluid was added into plenum (under the PPC plate), 6 L of cell fluid was added for sealing test, and finally the intracellular fluid in plenum was replaced with amphotericin B-containing intracellular fluid to establish a whole-cell recording mode after perforating sealed cells. The sampling frequency for recording TPRA1 current was 10 kHz, the cells were clamped at 0 mV, the voltage stimulation command (channel protocol) was a ramp voltage from −100 mV to +100 mV for 300 ms. This voltage stimulation was applied every 10 s, mTRPA1 current was induced by 300 M AITC.
Data recording and current amplitude measurement export were carried out by IWB software (version 2.5.3, Molecular Devices Corporation, Union City, Calif.). No statistics was recorded for holes with sealing impedance lower than 20 MΩ. The original current data was corrected by software for leakage reduction. TRPA1 current amplitude was measured at +100 mV. Each PPC plate in the experiment had a dose-effect data of HC030031 as a positive control. If IC50 value of HC030031 exceeded 3 times the average IC50 value previously obtained on each plate, it would be re-tested. The dose-effect curve of compounds and IC50 were fitted and calculated by GraphPad Prism 5.02 (GraphPad Software, San Diego, Calif.).
Some compounds of present invention were detected by IonWorks Barracuda (IWB) automated patch clamp detection method for IC50 inhibitory activity. The activity data was shown in Table 2, and the dose-effect relationship of some representative compounds in inhibiting TRPA1 activity was shown in
The results showed that the compounds of present invention exhibited potent inhibitory activity on TRPA1, wherein the IC50 values of 11 compounds on TRPA1 were 1-10 μM. It could be seen from
In addition, the test results of S configuration of compound IC-10 and the corresponding R configuration of compound i.e., (R)-3-(2,3-dihydro-1H-inden-4-yl)oxy)-N-methyl-3-(2-thienyl)-1-amine, and configuration of compound IC-23 and the corresponding R configuration of compound, i.e., (R)-3-(benzofuran-7-yloxy)-3-(thiophen-2-yl)propyl-1-amine showed that the ratio of IC50 of R configuration of compound to that of S configuration of compound was ≥2, which suggested that compounds of the present invention in S configuration had higher inhibitory activity on TRPA1.
In addition, the activity ratio of compound IC-10 (containing heteroaryl
to compound C1 (containing phenyl), i.e., the IC50 of compound C1/the IC50 of compound IC-10, was about 2.5-fold, which suggested that the compounds of present invention containing heteroaryl (such as compound IC-10) had higher inhibitory activity on TRPA1. In addition, compared with compounds with naphthalene ring as A group, such as duloxetine, the IC50 values of compound IC-10 with benzoalicyclic ring as A group, compound IC-3, compound IC-23, and compound IC-1 with benzoheteroaryl as A group were significantly decreased. Specifically, the ratio of the IC50 of S configuration of duloxetine to the IC50 of any of compound IC-10, compound IC-3, compound IC-23 or compound IC-1 was about 2.8-6.8 (note: the IC50 of R configuration of duloxetine was 48.5 μM, and the IC50 of S configuration of duloxetine was 24.74 μM). The results suggested that the compounds of present invention with benzoalicyclyl or heteroaryl as A group had higher (about 2.8-6.8 times higher) inhibitory activity on TRPA1.
Similarly, the inventors also measured the TRPA1 inhibitory activity of S configuration of duloxetine and compound IC-10 by manual patch clamp detection. Similar to the test results of automatic patch clamp detection method, in the manual patch clamp detection, the ratio of IC50 of the S configuration of duloxetine to the IC50 of the compound IC-10 was 4.36/1.12=3.9.
Similarly, the inventors also measured the TRPA1 inhibitory activity of compound IC-1 by manual patch clamp detection. The method was as follows:
The HEK293 cell line stably expressing human TRPA1 channel was placed in T75 culture flask with DMEM medium containing 15 μg/mL Blasticidin S HCl, 200 μg/mL Hygromycin B and 10% FBS, and cultured in incubator at 37° C. and 5% CO2. When the cell density reached about 80%, the culture medium was removed, the residue was rinsed with phosphate buffered saline (PBS) without calcium and magnesium. 2 mL of trypsin was added to digest for 2 minutes, and 8 mL of culture medium was added to terminate the digestion. The cells were collected to 15 mL centrifuge tube and centrifuged at 800 rpm for 3 min. After the supernatant was removed, an appropriate volume of extracellular fluid was added to re-suspend the cells.
In manual patch clamp detection, HEKA system (Patch Master software) was used together with EPC-10 amplifier to record the whole cell current of TRPA1 stably transfected cell line at room temperature. intracellular fluid formulation for whole cell recording was as follows (mM): 140 CsCl, 10 HEPES, 5 EGTA, 0.1 CaCl2, 1 MgCl2 (pH 7.2, osmotic pressure 295-300 mOsm); Ca2+-free extracellular fluid formulation for recording was as follows (mM): 140 NaCl, 5 KCl, 0.5 EGTA, 1 MgCl2, 10 Glucose, 10 HEPES (pH 7.4, osmotic pressure 300-310 mOsm). Glass microelectrode resistance used for patch clamp recording was 2-4 MΩ, the sampling frequency was 10 kHz, the filter frequency was 2.9 kHz, the cell clamp was 0 mV, and the voltage stimulation command (channel protocol) was a linear voltage from −100 mV to +100 mV for 300 ms, then restored to 0 mV clamping potential. The recording was performed every 2 s. The hTRPA1 current was induced by 100 μM AITC. To ensure the accuracy of current recording, the series resistance was used for 60% compensation during recording.
Data recording and current amplitude measurement export were completed by Patch Master software. Cells with sealing impedance lower than 500 MΩ, w were not included in the statistics. The original current data were corrected by software for leakage reduction, and the hTRPA1 current amplitude was measured at +100 mV. The compound dose-effect curve and IC50 were fitted and calculated by GraphPad Prism 5.02 (GraphPad Software, San Diego, Calif.).
The Results of Manual Patch Clamp Detection
Similar to the results of the automatic patch clamp detection, the ratio of IC50 of S configuration of duloxetine to that of compound IC-1 was 4.36 μM/0.43 μM=10.14 in the manual patch clamp detection.
Cytotoxicity Test
In this example, the method for determining hepatotoxicity and neurotoxicity of compound IC-10 and compound IC-1 were as follows:
HepG-2 and SH—SY5Y cells were placed in 10 cm dish and cultured at 37° C., 5% CO2 in a cell incubator. Trypsin was used to digest and resuspend cells and cells were counted. The cells were transferred to 96-well plate with 8000 cells in a well (100 μl/well). A serial of gradient concentration dilutions of compound with 2-fold dilution were prepared, and the system was 100 μL/well. The supernatant of cell culture system in the 96-well plate was removed on the first day, and fresh-prepared drug concentration system was add into culture plate wells (duplicate wells were set). The cells were cultured at 37° C., 5% CO2 in a cell incubator for 72 h. After the cell culture was completed, the supernatant of cell culture system was removed from 96-well plate, 100 μl of detection solution containing 10% CCK-8 medium was added into each well, and the cells were cultured at 37° C., 5% CO2 in a cell incubator for 1 h. Microplate reader was used to measure the absorbance at 450 nm. Data was processed to calculate cytotoxicity, and IC50 was calculated by GraphPad Prism. The cytotoxicity calculation formula was as follows: Cytotoxicity (%)=[A(0 Dosing)−A(Dosing)]/[A(0 Dosing)−A (control))×100
A (Dosing): the absorbance of wells containing cells, CCK-8 solution and drug solution.
A (control): the absorbance of wells containing medium and CCK-8 solution and without cells.
A (0 Dosing): the absorbance of wells containing cells and CCK-8 solution but without drug solution.
Experimental Result
The results of hepatotoxicity (HepG2 cell) and neurotoxicity (SH—SY5Y) of compound IC-10 and compound IC-1 showed: the hepatotoxicity and neurotoxicity of duloxetine were 33 μM and 28 μM (IC50, μM), respectively, while the hepatotoxicity and neurotoxicity of compound IC-1 and compound IC-10 of the present invention were about 60-120 μM (IC50, μM). It suggested that the toxicity and side effects of compounds of the present invention were significantly lower, and were about ½ or ⅓ of toxicity and side effects of duloxetine. The results showed the compounds of the present invention had excellent safety.
Analgesic Activity Test Experiment
In this example, analgesic activity of compound IC-10 of present invention was evaluated by mice formalin pain model. The method was as follows:
30 C57BL/6 mice (male, 9-week aged) were randomly divided into 3 groups: solvent control group (vehicle, saline), duloxetine group (duloxetine, 5-HT reuptake and NE reuptake inhibitor) and IC-10 group (compound IC-10 of the present invention). Before the start of experiment, the mice were allowed to adapt to the experimental environment for 72 h without fasting. The test drug was administrated by intraperitoneal injection at a dose of 20 mg/kg, and then the mice were placed in a transparent, ventilated plexiglass cylinder for 1 h, and then 20 μl of 4% formalin solution was injected into the left hind plantar of mice of each group by microinjector. The claw pain response of mice was real-time recorded by miniature camera. The number of times of lifting (1 min/time), shaking (2 min/time), and licking (3 min/time) left claw and the time length of licking left claw were used as indicators of pain response, the cumulative scoring and licking time in two stages of 0-10 min (phase I, acute pain phase) and 10-60 min (phase II, inflammatory pain phase) were observed and recorded, and the statistical analysis was conducted.
Experimental Results
The results of analgesic activity of compound IC-10 of the present invention in mice formalin pain model were shown in
Mice Hot Plate Pain Test Experiment
In this example, the analgesic activity of compound IC-23, compound IC-10, compound IC-1 and other compounds of the present invention were evaluated by C57 mice hot plate pain model. The method was as follows:
1 Animal Screening
SPF-grade C57 male mice were placed at hot plate with constant 55±0.1° C. Mice with painful response such as licking claw within 10-30 s were selected (the mice which evade and jump were abandoned). If the pain reaction of mice was observed, the mice were taken out immediately to prevent mice from scalding.
2 Animal Groups
The 40 selected animals were weighed and randomly divided into 4 groups: saline control group (blank control), duloxetine group (positive control group), gabapentin group (positive control group) and IC-23 group (compound of the present invention).
3 Sample Preparation
The test compounds were freshly prepared on the day of administration. 0.9% NaCl physiological saline solution was prepared as solvent for later use. Appropriate amount of test compounds were added into required volume of physiological saline and fully suspended, and the concentration of the drug compound in preparation was 1 mg/ml. The standard volume of administration to mice was 10 ml/kg (or 0.1 ml/10 g).
4 Animal Administration
The administration mode was intraperitoneal administration. animals did not need to fast before administration. The administration volume was 10 ml/kg. The dosage of duloxetine and IC-23 was 10 mg/kg, and the dosage of gabapentin was 100 mg/kg.
5 Hot Plate Experimental Observation
Hot plate observation index: the reaction time of mice on the hot plate at 55±0.1° C. (Time latency). Measurement and recording were conducted at 3 h before administration and 15 min, 30 min, and 60 min after administration.
6. Data Statistics and Analysis
Maximum possible effect (MPE) % was used to evaluate analgesic effect of each compound, i.e., MPE %=[(Post drug latency-baseline latency)/(30-baseline latency)]×100. MPE % at different time points was recorded. The higher the value of MPE % was, the stronger the analgesic effect of the compound was.
Experimental Results
The results of analgesic activity of compound IC-23 of the present invention in the mice hot plate pain model were shown in
Moreover, the analgesic activity of compound IC-10 and compound IC-1 were stronger than those of gabapentin and duloxetine at the same dose (10 mg/kg.
The hot plate pain model was a classic model for evaluating the efficacy of drugs on acute pain. Therefore, the compounds of the present invention had excellent therapeutic effect on acute pain.
Pharmacokinetic Test of Compound Ic-1
In this example, the pharmacokinetic properties of compounds such as duloxetine and compound Ic-1 were tested in rat. The method was as follows:
Test Method:
A certain amount of sample was weighed and dissolved in deionized water to prepare 1 mg/mL of solution. Male SD rats were used as test animals. The dose of single intravenous (IV) injection was 2 mg/kg, and the dose of oral (PO) administration was 10 mg/kg. Each group had three rats. The rats in oral group were fasted for 10-14 hours before administration, and were fed 4 hours after administration. Animal blood collection time points were as follows: before administration, and 5 min, 15 min, 30 min, 1 h, 2 h, 4 h, 6 h, 8 h, and 24 h after administration for intravenous administration; before administration, and 15 min, 30 min, 1 h, 2 h, 4 h, 6 h, 8 h and 24 h after administration for oral administration. About 0.25 mL of blood was collected via the jugular vein from each animal, and heparin sodium was used for anticoagulation. After collecting the blood samples, the blood samples were placed on ice and centrifuged to separate the plasma (centrifugation conditions: 8000 rpm, 6 min, 4° C.). The collected plasma was stored at −80° C. before analysis. 50 μL of plasma sample was taken into 1.5 mL of centrifuge tube, 250 μL of internal standard solution was added, and the same volume of methanol rather than internal standard solution was added in the blank group. The mixture was vortexed and mixed, centrifuged at 14,000 rpm for 5 min, 200 μL of supernatant was taken into 96-well sample plate, and the LC-MS/MS was used for sample analysis. In the linear regression analysis, the peak area was taken as the y-axis and the drug concentration was taken as the x-axis. The linear relationship between the peak area ratio and the concentration was expressed by the correlation coefficient (R) obtained from the regression equation of the compound. According to the blood concentration data of the drug, the pharmacokinetic calculation software WinNonlin7.0 non-compartmental model was used to calculate the pharmacokinetic parameters of the test drug.
Internal standard working solution: a certain amount of tolbutamide internal standard stock solution with a concentration of 490,000 ng/mL was taken into a volumetric flask with a certain volume, diluted to a desired volume with methanol and mixed well to obtain the internal standard working solution with a concentration of 200 ng/mL.
Experimental Results
According to average blood concentration data of drug in each group, the pharmacokinetic calculation software WinNonlin7.0 non-compartmental model was used to calculate pharmacokinetic parameters of compound in each group. The results were shown in Table 3.
Table 3 showed that after compound IC-1 was injected intravenously at a dose of 2 mg/kg, the peak concentration (Cmax, 170 ng/mL) was reached at the first time point of sampling (0.083 h), the elimination half-life (T1/2)) was 2.97 h, AUC(0-∞) was 449 h*ng/mL; after compound IC-1 was orally administered at a 5-fold dose (10 mg/kg), the peak concentration (Cmax, 266 ng/mL) was reached at 3 h, the elimination half-life (T1/2) was 5.69 h, and AUC(0-∞) was 4016 h*ng/mL. Based on the calculation on AUC (0-∞), the oral bioavailability was 179%.
After duloxetine was injected intravenously at a dose of 2 mg/kg, the peak concentration (Cmax, 177 ng/mL) was reached at 0.083 h, the elimination half-life (T1/2) was 1.77 h, and the AUC (0-∞) was 449 h*ng/mL; after duloxetine was orally administered at a 5-fold dose (10 mg/kg), the peak concentration (Cmax, 76 ng/mL) was reached at 0.83 h, the elimination half-life (T1/2) was 1.81 h, and the AUC (0-∞) was 222 h*ng/mL. Based on the calculation on AUC (0-∞), the oral bioavailability was 9.9%.
The results showed that, compared with duloxetine, the compounds of formula I of the present invention (such as compound IC-1) had more excellent pharmacokinetic properties with a longer half-life, higher exposure in plasma, and better bioavailability, so that it was suitable for development into a medicine for oral administration, and had a good prospect of medicine.
Evaluation of Therapeutic Effect of Compound IC-1 on Fibromyalgia in Mice ICS Model
Experimental Method
1. Experiment Group
The experimental groups were solvent control group, 10 mg/kg duloxetine group (positive control group) and 10 mg/kg compound IC-1 group (the compound prepared in Example 9)
2. Compound Preparation
10 mg/kg duloxetine: 17 mg of duloxetine was weighed, dissolved in saline and diluted to 8.5 mL. After completely dissolved, the duloxetine was administered orally. The volume of administration was 5 ml/kg.
10 mg/kg compound Ic-1:17 mg of compound Ic-1 was weighed, dissolved in saline and diluted to 8.5 mL. After completely dissolved, the compound Ic-1 was administered orally. The volume of administration was 5 ml/kg.
3. Animals
Male C57BL/6 mice weighed 18-22 g were selected at the beginning of experiment. Each cage had 4 mice which were allowed to feed and drink water freely. Each experimental group had 12 mice, and the experimental mice were labeled by tail labeling method.
4. Experimental Method
4.1 Model Establishment
Day 0: At 4:30 pm, the mice were put in a plexiglass box with stainless steel mesh, and then the plexiglass box was put in cold environment (4±2° C.) overnight. The mice were allowed to feed freely and drink, and agar was used to replace water.
Day 1: At 10:00 am, the mice were delivered to room temperature (24±2° C.) environment for 30 min, and then the mice were delivered to cold environment for 30 min. The above steps were repeated until 4:30 μm, and the mice were put in cold environment overnight.
Day 2: the operation on day 1 was repeated.
Day 3: the mice were taken out from cold environment at 10:00 am.
4.2 Administration
The compounds were administered orally according to the schedule of experiment, and the dosage was 10 mg/kg.
4.3 Mechanical Allodynia Test
On the fourth day after modeling, the pre-administration mechanical allodynia test was performed on the animals. Animals with PWT value greater than 0.5 g were excluded and were not used for experiments. On the fifth day after modeling, the animals were tested for mechanical allodynia at 0.5 h, 1 h, and 2 h after the administration of compounds.
The Test Method for Mechanical Allodynia was as Follows:
The mice was individually placed in a plexiglass box with a grid on the bottom of the box to ensure that the mice claw could be tested. The mice were allowed to adapt for 15 min before the test. After the adaptation was completed, the test fiber was used to test the center of the left hind claw of mice. The test fiber comprised 8 test strengths: 2.36 (0.02 g), 2.44 (0.04 g), 2.83 (0.07 g), 3.22 (0.16 g), 3.61 (0.4 g), 3.84 (0.6 g), 4.08 (1 g), and 4.17 (1.4 g). During the test, the test fiber was pressed vertically against the skin and forced to bend for 6-8 s with a 5 s interval of test.
During the test, rapid withdrawal of animal claw was recorded as pain response. When the test fiber was removed from animal skin, the withdrawal of animal claw was also recorded as pain response. If animal moved, the pain response was not recorded, and the test was repeated. In the test, 3.22 (0.16 g) was used firstly. If animal responded to pain, the test fiber with lower strength was used in next test; if the animal did not respond to pain, test fiber with higher strength was used in next test (Chaplan et al. 1994). The maximum strength of tested fiber was 4.17 (1.4 g).
5. Data Collection and Analysis
Excel software was used to collect data, and prism software was used to analyze data. The larger the withdrawal threshold (PWT) was, the stronger the analgesic effect of the compound was.
Experimental Result
The results of analgesic activity of compound Ic-1 in the mice ICS model were shown in Table 5 and
The Table 5 and
Evaluation of Therapeutic Effect of Compound IC-1 on Visceral Pain and Inflammatory Pain in Mice Acetic Acid Writhing Pain Model
Experimental Method
Male ICR mice, weighed 22-25 g, were fasted but allowed to drink water freely for 2 h before administration. All ICR mice were weighed and grouped randomly, and the number of animals in each group was >10. The negative control group was saline group (vehicle, blank control), and the positive control group was administrated with 10 mg/kg indomethacin (a non-steroidal anti-inflammatory drug), 10 mg/kg anisodamine (an antispasmodic drug with clinically analgesic activity), 10 mg/kg duloxetine and 20 mg/kg duloxetine. The test compound was IC-1 (the compound prepared in Example 9), and the administration dosages were 5 mg/kg and 10 mg/kg. The drug was administrated by gavage based on the weight of mice. 1.5% acetic acid solution (0.1 ml/10 g) was injected intraperitoneally 1 hour after administration, and the number of times of visceral pain in each group was observed within 30 min. When concave abdomen, stretched trunk and hind claw, and high buttocks appeared, one number point was recorded. Finally, the number of appearance of the above phenomenon was counted within 30 minutes. After administration, the fewer visceral pains in the mice were, the stronger the analgesic effect of the compound was.
Experimental Result
The mice acetic acid writhing pain model test results were shown in
This experiment showed that the analgesic activity of compound IC-1 of the present invention was significantly stronger than positive control drug in the mice acetic acid writhing pain model. The mice acetic acid writhing pain model was a classical model for evaluating the efficacy of drug in treating visceral pain and inflammatory pain. Therefore, the compound IC-1 of the present invention had excellent therapeutic effect on visceral pain and inflammatory pain.
Evaluation of Therapeutic Effect of Compound IC-1 on Nerve Pain in Rat SNL Model
Experimental Method
Male SPF grade SD rats, weighed 150-180 g, were selected. Aseptic operation during surgery was performed. The animals were anesthetized with sodium pentobarbital (50 mg/kg, intraperitoneal injection). The surgical area of animal waist was shaved and the skin was disinfected three times with iodophor and 70% ethanol. After the skin was dried, the operation was started. Surgical knife was used to make a longitudinal incision at the back of the sacrum of the animal waist to expose the left paraspinal muscles, and stretcher was used to separate muscle tissue to expose the spine. The left spinal nerves L5 and L6 were separated and ligated with a 6-0 silk thread, and the wound was sutured. After the operation, the animals were placed on electrothermal pad, and 5 mL of saline was injected subcutaneously to prevent dehydration. After the animals were fully awakened and could move around freely, the animals were put back in the cage.
After the operation, the animals were adapted in the experimental environment for 15 min/day for 3 days. One day before the administration, the rats were subjected to mechanical allodynia baseline test, and the animals that did not exhibit mechanical allodynia (the withdrawal threshold was greater than 5 g) were eliminated and the remaining rats were randomly divided into one control group and two experimental groups.
The animals were weighed to calculate the dosage. The rats in two experimental groups were administrated with 100 mg/kg gabapentin (gabapentin was currently the first-line drug for the treatment of neuralgia) and 10 mg/kg compound IC-1 (the compound prepared in Example 9), and the rats in control group were administrated with equal volume of saline orally. 1 h after administration, mechanical allodynia test was performed. The rat was individually placed in a plexiglass box with a grid on the bottom of the box to ensure that the rat claw could be tested. The rats were allowed to adapt the environment for 15 min before test. After the adaptation was completed, the test fiber was used to test the center of the left hind claw of the rat. The test fiber comprises 8 test strengths: 3.61 (0.4 g), 3.84 (0.6 g), 4.08 (1 g), 4.31 (2 g), 4.56 (4 g), 4.74 (6 g), 4.93 (8 g), 5.18 (15 g). During the test, the test fiber was pressed vertically against the skin and forced to bend the fiber for 6-8 s with a 5 s interval of test. During the test, rapid withdrawal of animal claw was recorded as pain response. When the test fiber was removed from animal skin, the withdrawal of animal claw was also recorded as pain response. If animal moved, the pain response was not recorded and the test was repeated. In the test, 4.31 (2 g) was used firstly. If animal responded to pain, the test fiber with lower strength was used in next test; if the animal did not respond to pain, test fiber with higher strength was used in next test. The maximum strength of tested fiber was 5.18 (15 g).
Mechanical allodynia was expressed as withdrawal threshold (PWT) in rat behavioral test, which was calculated with the following formula:
50% response threshold(g)=(10(Xf+kδ))/10,000;
Excel software was used to collect data, and Prism 6.01 (Graph pad software, Inc.) software was used to analyze data. The larger the withdrawal threshold (PWT) was, the stronger the analgesic effect of the compound was.
Experimental Result
The results of analgesic activity in the rat SNL model were shown in Table 6 and
Table 6 and
Evaluation of Therapeutic Effect of Compound IC-1 on Acute Pain and Inflammatory Pain in Mice Formalin Pain Model
Experimental Method
100 male C57BL/6 mice (9-week aged), were randomly divided into 10 groups to evaluate analgesic activity of two compounds in the mice formalin pain model, and each group had 10 mice. The experimental groups were duloxetine group and the compound Ic-1 group (the compound prepared in Example 9), respectively. Before the start of experiment, the mice were allowed to adapt experimental environment for 72 h with free feeding and drinking water. The test drug was administrated intraperitoneally, and the dosage was as follows:
Duloxetine group: blank vehicle (blank saline control), 1 mg/kg, 5 mg/kg, 10 mg/kg and 20 mg/kg;
Compound Ic-1 group: blank vehicle (blank saline control, similar to that in Duloxetine group), 0.1 mg/kg, 0.5 mg/kg, 1 mg/kg, 5 mg/kg and 10 mg/kg.
After administration, the mice were placed in a transparent, ventilated plexiglass cylinder, and 1 h later, 20 μl of 4% formalin solution was injected into the left hind plantar of mice in each group by micro-injector, and claw pain response in mice was recorded in real time by a mini-camera. The time length of licking left claw was used as an indicator of pain response, licking time in 0-10 min (phase I) and 10-60 min (phase II) was observed and recorded, and the statistical analysis was conducted. The half effective dose (ED50) of three compounds was calculated: ED50 referred to the dose of the drug that decreased licking time by half as compared with the blank control group. The smaller the ED50 value was, the lower the effective analgesic dose of the compound was and the stronger the analgesic effect was.
Experimental Results
The claw licking time statistical results of compound Ic-1 and duloxetine in the mice formalin model at different dosages (10-60 min) were shown in Table 7 and
Table 7 and
All documents mentioned in the present invention are incorporated herein by reference, as if each document is individually cited for reference. It should be understood that those skilled in the art will be able to make various changes or modifications to the present invention after reading the teachings of the present invention, which also fall within the scope of the claims appended hereto.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201810942562.6 | Aug 2018 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2019/101197 | 8/16/2019 | WO | 00 |
