WO2003049741A1 - Ureas of 2-aminobenzothiazoles as adenosine modulators - Google Patents

Ureas of 2-aminobenzothiazoles as adenosine modulators Download PDF

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WO2003049741A1
WO2003049741A1 PCT/EP2002/013761 EP0213761W WO03049741A1 WO 2003049741 A1 WO2003049741 A1 WO 2003049741A1 EP 0213761 W EP0213761 W EP 0213761W WO 03049741 A1 WO03049741 A1 WO 03049741A1
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methoxy
benzothiazol
morpholin
aza
amide
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PCT/EP2002/013761
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French (fr)
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Alexander Flohr
Roland Jakob-Roetne
Roger David Norcross
Claus Riemer
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F. Hoffmann-La Roche Ag
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Priority to KR1020047008868A priority Critical patent/KR100659793B1/en
Priority to BR0214825-0A priority patent/BR0214825A/en
Priority to MXPA04005444A priority patent/MXPA04005444A/en
Priority to CA002469596A priority patent/CA2469596A1/en
Priority to DE60219682T priority patent/DE60219682T2/en
Priority to ES02804578T priority patent/ES2283652T3/en
Priority to JP2003550790A priority patent/JP4245483B2/en
Priority to EP02804578A priority patent/EP1455792B1/en
Priority to AU2002356626A priority patent/AU2002356626B2/en
Publication of WO2003049741A1 publication Critical patent/WO2003049741A1/en

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Definitions

  • Preferred compounds ofthe present application for use against diseases, related to the A 2a receptor are compounds of formula I, wherein X is -O-, for example the following compounds:

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Abstract

The present invention relates to the use of compounds of the general formula (I) and to pharmaceutically acceptable acid addition salts thereof for the manufacture of medicaments for the treatment of diseases, related to the adenosine A2 receptor system like Alzheimer's disease, Parkinson disease, anxiety pain and other neurological disorders.

Description

UREAS OF 2-AMINOBENZOTHIAZO ES AS ADENOSINE MODULATORS
The present invention relates to the use of compounds ofthe general formula
Figure imgf000002_0001
wherein
R is lower alkoxy or halogen;
R'/R2 are independently from each other hydrogen, lower alkyl, tetrahydropyran-4-yl or cycloalkyl, which is unsubstituted or substituted by one or two substituents, selected from the group consisting of halogen, lower alkoxy or hydroxy, or
R1 and R" form together with the N atom to which they are attached heterocyclic rings, selected from the group consisting of 2-oxa-5-aza-bicyclo [2.2.1] heptane,
3-endo-hydroxy-8-aza-bicyclo[3.2.1] octane,
2-aza-bicyclo [2.2.2] octane, l-oxo-2,8-diaza-spiro[4.5] decane,
3-aza-spiro[5.5]undecane, 8-aza-spiro[4.5]decane, l-oxa-8-aza-spiro[4.5]decane,
1, 8, 8-trimethyl-3-aza-bicyclo[3.2.1 ] octane,
[ l,4]oxazepane,
2-oxa-5-aza-bicyclo [2.2.2] octane, 8-oxa-3-aza-bicyclo [3.2.1] octane,
1,4-diaza-bicyclo [3.2.1] octane,
2-aza-bicyclo [2.2.1] heptane,
3-aza-bicyclo[3.2.1] octane, which rings may be unsubstituted or substituted by lower alkyl, or is selected from piperazinyl, unsubstituted or mono or di-substituted by lower alkyl, phenyl or oxo, or is selected from piperidin-1-yl, substituted by -(CH2)n-NR'S(O)2-lower alkyl, -C(O)NR'2or -(CH )„-phenyl, wherein the phenyl ring is unsubstituted or substituted by lower alkyl; R' is hydrogen or lower alkyl, independently from each other in case R'2;
X is -O- or -CH2- and
n is 0, 1, 2, 3 or 4 and to pharmaceutically acceptable acid addition salts thereof for the manufacture of medicaments for the treatment of diseases, related to the adenosine A2 receptor system. Such diseases include Alzheimer's disease, Parkinson's disease, Huntington's disease, neuroprotection, schizophrenia, anxiety, pain, respiration deficits, depression, drug addiction, such as amphetamine, cocaine, opioids, ethanol, nicotine, cannabinoids, or against asthma, allergic responses, hypoxia, ischaemia, seizure and substance abuse. Furthermore, compounds ofthe present invention maybe useful as sedatives, muscle relaxants, antipsychotics, antiepileptics, anticonvulsants and cardiaprotective agents for disorders such as coronary artery disease and heart failure. The most preferred indications in accordance with the present invention are those, which base on the A2A receptor antagonistic activity and which include disorders ofthe central nervous system, for example the treatment or prevention of Alzheimer's disease, certain depressive disorders, drug addiction, neuroprotection and Parkinson's disease as well as ADHD.
It has surprisingly been found that the compounds of general formula I are adenosine receptor ligands. Specifically, the compounds ofthe present invention have a good affinity to the A2A-receptor and a high selectivity to the Ai- and A3 receptors.
Adenosine modulates a wide range of physiological functions by interacting with specific cell surface receptors. The potential of adenosine receptors as drug targets was first reviewed in 1982. Adenosine is related both structurally and metabolically to the bioactive nucleotides adenosine triphosphate (ATP), adenosine diphosphate (ADP), adenosine monophosphate (AMP) and cyclic adenosine monophosphate (cAMP); to the biochemical methylating agent S-adenosyl-L-methione (SAM); and structurally to the coenzymes NAD, FAD and coenzym A; and to RNA. Together adenosine and these related compounds are important in the regulation of many aspects of cellular metabolism and in the modulation of different central nervous system activities. The receptores for adenosine have been classified as Ai, A2A, A2B and A3 receptors, belonging to the family of G protein-coupled receptors. Activation of adenosine receptors by adenosine initiates signal transduction mechanism. These mechanisms are dependent on the receptor associated G protein. Each ofthe adenosine receptor subtyps has been classically characterised by the adenylate cyclase effector system, which utilises cAMP as a second messenger. The Ai and A3 receptors, coupled with G; proteins inhibit adenylate cyclase, leading to a decrease in cellular cAMP levels, while A2A and A2B receptors couple to Gs proteins and activate adenylate cyclase, leading to an increase in cellular cAMP levels. It is known that the Ai receptor system include the activation of phospholipase C and modulation of both potassium and calcium ion channels. The A3 subtype, in addition to its association with adenylate cyclase, also stimulates phospholipase C and so activates calcium ion channels.
The Ai receptor (326-328 amino acids) was cloned from various species (canine, human, rat, dog, chick, bovine, guinea-pig) with 90-95 % sequence identify among the mammalian species. The A2A receptor (409-412 amino acids) was cloned from canine, rat, human, guinea pig and mouse. The A2B receptor (332 amino acids) was cloned from human and mouse with 45 % homology of human A2B with human Ai and A2A receptors. The A3 receptor (317-320 amino acids) was cloned from human, rat, dog, rabbit and sheep.
The Ai and A2A receptor subtypes are proposed to play complementary roles in adenosine's regulation ofthe energy supply. Adenosine, which is a metabolic product of ATP, diffuses from the cell and acts locally to activate adenosine receptors to decrease the oxygen demand (Aj) or increase the oxygen supply (A2A) and so reinstate the balance of energy supply: demand within the tissue. The actions of both subtyps is to increase the amount of available oxygen to tissue and to protect cells against damage caused by a short term imbalance of oxygen. One ofthe important functions of endogenous adenosine is preventing damage during traumas such as hypoxia, ischaemia, hypotension and seizure activity.
Furthermore, it is known that the binding ofthe adenosine receptor agonist to mast cells expressing the rat A3 receptor resulted in increased inositol triphosphate and intracellular calcium concentrations, which potentiated antigen induced secretion of inflammatory mediators. Therefore, the A3 receptor plays a role in mediating asthmatic attacks and other allergic responses.
Adenosine is a neuromodulator, able to modulate many aspects of physiological brain function. Endogenous adenosine, a central link between energy metabolism and neuronal activity, varies according to behavioural state and (patho)physiological conditions. Under conditions of increased demand and decreased availability of energy (such as hypoxia, hypoglycemia, and/or excessive neuronal activity), adenosine provides a powerful protective fedback mechanism. Interacting with adenosine receptors represents a promising target for therapeutic intervention in a number of neurological and psychiatric diseases such as epilepsy, sleep, movement disorders (Parkinson or Huntington's disease), Alzheimer's disease, depression, schizophrenia, or addiction An increase in neurotransmitter release follows traumas such as hypoxia, ischaemia and seizures. These neurotransmitters are ultimately responsible for neural degeneration and neural death, which causes brain damage or death of the individual. The adenosine Ai agonists which mimic the central inhibitory effects of adenosine may therefore be useful as neuroprotective agents. Adenosine has been proposed as an endogenous anticonvulsant agent, inhibiting glutamate release from excitory neurons and inhibiting neuronal firing. Adenosine agonists therefore maybe used as antiepileptic agents. Adenosine antagonists stimulate the activity ofthe CNS and have proven to be effective as cognition enhancers. Selective A2a antagonists have therapeutic potential in the treatment of various forms of dementia, for example in Alzheimer's disease, and of neurodegenerative disorders, e.g. stroke. Adenosine A2a receptor antagonists modulate the activity of striatal GABAergic neurons and regulate smooth and well-coordinated movements, thus offering a potential therapy for Parkinsonian symptoms. Adenosine is also implicated in a number of physiological processes involved in sedation, hypnosis, schizophrenia, anxiety, pain, respiration, depression, and drug addiction (amphetamine, cocaine, opioids, ethanol, nicotine, cannabinoids). Drugs acting at adenosine receptors therefore have therapeutic potential as sedatives, muscle relaxants, antipsychotics, anxiolytics, analgesics, respiratory stimulants, antidepressants, and to treat drug abuse. They may also be used in the treatment of ADHD (attention deficit hyper-activity disorder).
An important role for adenosine in the cardiovascular system is as a cardioprotective agent. Levels of endogenous adenosine increase in response to ischaemia and hypoxia, and protect cardiac tissue during and after trauma (preconditioning). By acting at the Ai receptor, adenosine Ai agonists may protect against the injury caused by myocardial ischemia and reperfusion. The modulating influence of A2a receptors on adrenergic function may have implications for a variety of disorders such as coronary artery disease and heart failure. A2a antagonists may be of therapeutic benefit in situations in which an enhanced antiadrenergic response is desirable, such as during acute myocardial ischemia. Selective antagonists at A2a receptors may also enhance the effectiveness of adenosine in terminating supraventricula arrhytmias.
Adenosine modulates many aspects of renal function, including renin release, glomerular filtration rate and renal blood flow. Compounds which antagonise the renal affects of adenosine have potential as renal protective agents. Furthermore, adenosine A3 and/or A2B antagonists maybe useful in the treatment of asthma and other allergic responses or and in the treament of diabetes mellitus and obesity.
Numerous documents describe the current knowledge on adenosine receptors, for example the following publications:
Bioorganic & Medicinal Chemistry, 6, (1998), 619-641,
Bioorganic & Medicinal Chemistry, 6, (1998), 707-719,
J. Med. Chem., (1998), 41, 2835-2845,
J. Med. Chem., (1998), 41, 3186-3201,
J. Med. Chem., (1998), 41, 2126-2133, J. Med. Chem., (1999), 42, 706-721,
J. Med. Chem., (1996), 39, 1164-1171,
Arch. Pharm. Med. Chem., 332, 39-41, (1999),
Am. J. Physiol, 276, H1113-1116, (1999) or
Naunyn Schmied, Arch. Pharmacol. 362, 375-381, (2000).
Furthermore, WO 01/57008 describes benzothiazolyl urea derivatives and their use as protein kinase inhibitors. These compounds are useful as inhibitors of tyrosine kinases that are important in hyper-proliferative diseases, especially in cancer and in the process of angiogenesis. The following compounds of formulae IA and IB are not encompassed by WO 01/57008.
Therefore, the present invention relates also to novel compounds of formula IA
Figure imgf000006_0001
wherein
R is lower alkoxy or halogen;
R11 and R21 form together with the N atom to which they are attached heterocyclic rings, selected from the group consisting of 2-oxa-5-aza-bicyclo[2.2.1]heptane, 3-endo-hydroxy-8-aza-bicyclo[3.2.1] octane, 2-aza-bicyclo [2.2.2] octane, l-oxo-2,8-diaza-spiro[4.5]decane,
3-aza-spiro[5.5]undecane,
8-aza-spiro[4.5]decane, l-oxa-8-aza-spiro [4.5] decane, l,8,8-trimethyl-3-aza-bicyclo[3.2.1]octane,
[l,4]oxazepane,
2-oxa-5-aza-bicyclo [2.2.2] octane,
8-oxa-3-aza-bicyclo [3.2.1] octane,
1,4-diaza-bicyclo [3.2.1] octane,
2-aza-bicyclo[2.2.1]heptane>
3-aza-bicyclo [3.2.1] octane, which rings may be unsubstituted or substituted by lower alkyl, or is selected from piperidin-1-yl, substituted by -(CH2)n-NR'S(O)2-lower alkyl, -C(O)NR'2or
-(CH2)n-phenyl, wherein the phenyl ring is unsubstituted or substituted by lower alkyl;
R' is hydrogen or lower alkyl, independently from each other in case R'2;
X is -O- or CH2-; and
n is 0, 1, 2, 3 or 4
and to pharmaceutically acceptable acid addition salts thereof.
The present invention relates also to novel compounds of formula IB
Figure imgf000007_0001
wherein
R is lower alkoxy or halogen;
R12 is lower alkyl and R22 is cycloalkyl, substituted by one or two substituents, wherein the substituents are selected from the group, consisting of halogen, lower alkoxy or hydroxy;
X is -O- or CH2-;
Novel compounds of formula IA , wherein X is -O-, are, for example, the following:
( lS,4S)-2-oxa-5-aza-bicyclo[2.2.1]heptane-5-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
3-eπrfo-hydroxy-8-aza-bicyclo [3.2. l]octane-8-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
2-methyl-l-oxo-2,8-diaza-spiro[4.5]decane-8-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzofhiazol-2-yl)-amide,
1 -oxo-2,8-diaza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide,
4-benzyl-4-hydroxymethyl-piperidine-l -carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide, 3-aza-spiro[5.5]undecane-3-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-
2-yl)-amide,
8-aza-spiro[4.5]decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2- yl) -amide,
2-aza-bicyclo [2.2.2] octane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol- 2-yl) -amide,
1 -oxa-8-aza-spiro [4.5] decane- 8 -carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide,
(J?)-4-(l-hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide, (S)-4-(l-hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide,
4- ( methanesulfonylamino-methyl) -piperidine- 1-carboxylic acid (4-methoxy-7- morpholin-4-yl-benzothiazol-2-yl)-amide, piperidine- 1,4-dicarboxylic acid 4-amide l-[(4-methoxy-7-morpholin-4-yl-benzothiazol- 2-yl)-amide],
(lR)-l,8,8-trimethyl-3-aza-bicyclo[3.2.1]octane-3-carboxylic acid (4-methoxy-7- morpholin-4-yl-benzothiazol-2-yl)-amide,
2-oxa-5-aza-bicyclo[2.2.2]octane-5-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide, l,4-diaza-bicyclo[3.2.1]octane-4-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide or (lS,4R)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide.
Novel compounds of formula IA are also those, wherein X is -CH2, for example, the following: l-oxa-8-aza-spiro[4.5]decane-8-carboxylic acid (4-methoxy-7-piperidin-lyl-benzothiazol-
2-yl)-amide,
4-hydroxy-4-(4-methyl-benzyl)-piperidine-l-carboxylic acid (4-chloro-7-piperidin-l-yl- benzothiazol-2-yl) -amide or
4-benzyl-piperidine- 1-carboxylic acid (4-chloro-7-piperidin- l-yl-benzothiazol-2-yl)- amide.
Novel compounds of formula IB, wherein X is -O-, are, for example, the following:
1 - (4czs-fluoro-cyclohexyl) -3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)- 1 -methyl- urea, l-(4,4-difluoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
(cis)-l-(4-methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
(frajιs)-l-(4-hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea, (ds)-l-(4-hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea or
(traπs)-l-(4-methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea.
Objects ofthe present invention are the compounds of formula IA or IB per se, the use of compounds of formula I and their pharmaceutically acceptable salts for the manufacture of medicaments for the treatment of diseases, related to the adenosine A2 receptor, their manufacture, medicaments based on a compound in accordance with the invention and their production as well as the use of compounds of formula I in the control or prevention of illnesses based on the modulation of the adenosine system, such as Alzheimer's disease, Parkinson's disease, Huntington's disease, neuroprotection, schizophrenia, anxiety, pain, respiration deficits, depression, drug addiction, such as amphetamine, cocaine, opioids, ethanol, nicotine, cannabinoids, or against asthma, allergic responses, hypoxia, ischaemia, seizure and substance abuse. Furthermore, compounds of the present invention may be useful as sedatives, muscle relaxants, antipsychotics, antiepileptics, anticonvulsants and cardiaprotective agents for disorders such as coronary artery disease and heart failure. The most preferred indications in accordance with the present invention are those, which base on the A2 receptor antagonistic activity and which include disorders ofthe central nervous system, for example the treatment or prevention of Alzheimer's disease, certain depressive disorders, drug addiction, neuroprotection and Parkinson's disease as well as ADHD.
As used herein, the term "lower alkyl" denotes a saturated straight- or branched- chain alkyl group containing from 1 to 6 carbon atoms, for example, methyl, ethyl, propyl, isopropyl, n-butyl, i-butyl, 2 -butyl, t-butyl and the like. Preferred lower alkyl groups are groups with 1 - 4 carbon atoms.
The term "halogen" denotes chlorine, iodine, fluorine and bromine.
The term "lower alkoxy" denotes a group wherein the alkyl residues is as defined above, and which is attached via an oxygen atom.
The term "pharmaceutically acceptable acid addition salts" embraces salts with inorganic and organic acids, such as hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid, citric acid, formic acid, fumaric acid, maleic acid, acetic acid, succinic acid, tartaric acid, methane-sulfonic acid, p-toluenesulfonic acid and the like.
Preferred compounds ofthe present application for use against diseases, related to the A2a receptor are compounds of formula I, wherein X is -O-, for example the following compounds:
(lS,4S)-2-oxa-5-aza-bicyclo[2.2.1]heptane-5-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
3-eπrfo-hydroxy-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
2-methyl-l-oxo-2,8-diaza-spiro[4.5]decane-8-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide, l-oxo-2,8-diaza-spiro[4.5]decane-8-carboxylic acid (4-methoxy~7-morpholin-4-yl- benzothiazol-2-yl)-amide,
4-benzyl-4-hydroxymethyl-piperidine-l -carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
3-aza-spiro[5.5]undecane-3-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol- 2-yl) -amide,
8-aza-spiro[4.5]decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2- yl) -amide,
2-aza-bicyclo [2.2.2] octane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-
2-yl) -amide, 1 -oxa-8-aza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide,
(#)-4-( l-hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide, (S)-4-(l-hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
4-(methanesulfonylamino-methyl)-piperidine-l-carboxylic acid (4-methoxy-7- morpholin-4-yl-benzothiazol-2-yl)-amide, piperidine- 1,4-dicarboxylic acid 4-amide l-[(4-methoxy-7-morpholin-4-yl-benzothiazol- 2-yl)-amide], l-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-3-(tetrahydro-pyran-4-yl)-urea,
4-isopropyl-piperazine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2- yl) -amide,
4-phenyl-piperazine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)- amide, l-cyclohexyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea, l-(4αs-fluoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl- urea, l-(4cis-fiuoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl- urea,
( 's)-l-(4-methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
(trø7is)-l-(4-hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- mefhyl-urea, [l,4]oxazepane-4-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)- amide,
(αs)-l-(4-hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
2-oxa-5-aza-bicyclo [2.2.2] octane-5-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
(tr πs)-l-(4-methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
(lS,4R)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide, 3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-l-(tetrahydro-pyran-4-yl)- urea, l-cycloheptyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea, l-cyclopentyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea or l-cyclopentyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-urea. Preferred compounds ofthe present application for use against diseases, related to the A2a receptor are also compounds of formula I, wherein X is -CH2-, for example the following compounds: l-oxa-8-aza-spiro[4.5] decane-8-carboxylic acid (4-methoxy-7-piperidin-lyl-benzothiazol- 2-yl)-amide,
4-hydroxy-4-(4-methyl-benzyl)-piperidine-l-carboxylic acid (4-chloro-7-piperidin-l-yl- b enzothiazol-2 -yl) -amide,
4-benzyl-piperidine-l-carboxylic acid (4-chloro-7-piperidin-l-yl-benzothiazol-2-yl)- amide, 4-methyl-3-oxo-piperazine-l -carboxylic acid (4-methoxy-7-piperidin-l-yl-benzothiazol-
2-yl)-amide or l-(4-chloro-7-piperidin-l-yl-benzothiazol-2-yl)-3-cyclohexyl-urea.
The present compounds of formula IA or IB and their pharmaceutically acceptable salts can be prepared by methods known in the art, for example, by processes described below, which process comprises
a) reacting a compound of formula
Figure imgf000012_0001
with phenyl chloroformate and then with a compound of formula
HNRUR21 (3A) or HNR12R22 (3B)
to a compound of formula
Figure imgf000012_0002
wherein R and X are as defined above, and R and R >21 form together with the N atom to which they are attached heterocyclic rings, selected from the group consisting of 2-oxa-5-aza-bicyclo[2.2.1]heptane, 3-endo-hydroxy-8-aza-bicyclo[3.2.1]octane, 2-aza-bicyclo [2.2.2] octane, l-oxo-2,8-diaza-spiro[4.5]decane, 3-aza-spiro[5.5]undecane, 8-aza-spiro[4.5]decane, l-oxa-8-aza-spiro[4.5]decane, l,8,8-trimethyl-3-aza- bicyclo[3.2.1]octane, [ 1,4] oxazepane, 2-oxa-5-aza-bicyclo [2.2.2] octane, 8-oxa-3-aza-bicyclo[3.2.1]octane, l,4-diaza-bicyclo[3.2.1]octane, 2-aza-bicyclo [2.2.1] heptane or 3-aza-bicyclo [3.2.1] octane, and which rings maybe unsubstituted or substituted by lower alkyl, or is selected from piperidin-1-yl, substituted by -(CH2)n-phenyi, -(CH2)n-NR'S(O)2-lower alkyl, -C(O)NR'2 or -(CH2)n-phenyl and wherein the phenyl ring is unsubstituted or substituted by lower alkyl and R' is hydrogen or lower alkyl, independently from each other in case R'2 and n is described above, and R12 is alkyl and R is cycloalkyl, substituted by one or two substituents, wherein the substituents are selected from the group, consisting of halogen, lower alkoxy or hydroxy; or
if desired, converting the compounds obtained into pharmaceutically acceptable acid addition salts.
The compounds of formula IA and IB maybe prepared in accordance with process variant a) and with the following scheme 1. Scheme 2 shows the preparation ofthe intermediate compound of formula (2). 37 Examples are further described in more detail for the preparation of compounds of formula I A and IB.
Scheme 1
Figure imgf000013_0001
wherein the substituents are described above.
Preparation of a compound of formula IA or IB To a solution of a compound of formula (2), for example 4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl-amine in dichloromethane is subsequently added pyridine and phenyl chloroformate and the resulting solution is stirred for 45 min at ambient temperature. Then a compound of formula (3A) or (3B), for example (lS,4S)-2-oxa-5-aza- bicyclo[2.2.1]heptane is added and the mixture stirred at ambient temperature for about 15 min and at 40 °C for 2.5 h. After cooling to ambient temperature, saturated aqueous sodium carbonate is added, the organic phase is separated and dryed.
The preparation ofthe starting compound of formula (2) has been described in EP 00113219.0 as follows:
Figure imgf000014_0001
Figure imgf000014_0002
wherein the numbers 1 - 5 have the following meaning
1 morpholine or piperidine, base, Pd-catalyst,
2 H2 and Pd-C, or H2 and Raney-Ni, or TiCl3, or Fe, 3 Ph(CO)NCS,
4 NaOMe,
5 Br2.
R is lower alkoxy or halogen and R' is piperidin-1-yl or morpholinyl.
Isolation and purification ofthe compounds
Isolation and purification ofthe compounds and intermediates described herein can be effected, if desired, by any suitable separation or purification procedure such as, for example, filtration, extraction, crystallization, column chromatography, thin-layer chromatography, thick-layer chromatography, preparative low or high-pressure liquid chromatography or a combination of these procedures. Specific illustrations of suitable separation and isolation procedures can be had by reference to the Preparations and Examples herein below. However, other equivalent separation or isolation procedures could, of course, also be used.
Salts of compounds of formula IA or IB
The basic groups of compounds of formula IA or IB maybe converted to a corresponding acid addition salt. The conversion is accomplished by treatment with at least a stoichiometric amount of an appropriate acid, such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like, and organic acids suchas acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, malic acid, malonic acid, succinic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like. Typically, the free base is dissolved in an inert organic solvent such as diethyl ether, ethyl acetate, chloroform, ethanol or methanol and the like, and the acid added in a similar solvent. The temperature is maintained between 0 °C and 50 °C. The resulting salt precipitates spontaneously or maybe brought out of solution with a less polar solvent.
The acid addition salts ofthe basic compounds of formula I may be converted to the corresponding free bases by treatment with at least a stoichiometric equivalent of a suitable base such as sodium or potassium hydroxide, potassium carbonate, sodium bicarbonate, ammonia, and the like.
The compounds of formula I and their pharmaceutically usable addition salts possess valuable pharmacological properties. Specifically, it has been found that the compounds of the present invention are adenosine receptor ligands and possess a high affinity towards the adenosine A2A receptor and a good selectivity towards Ai and A3 receptors.
The compounds were investigated in accordance with the test given hereinafter.
Human adenosine A?A receptor
The human adenosine A2A receptor was recombinantly expressed in Chinese hamster ovary (CHO) cells using the semliki forest virus expression system. Cells were harvested, washed twice by centrifugation, homogenised and again washed by centrifugation. The final washed membrane pellet was suspended in a Tris (50 mM) buffer containing 120 mM NaCI, 5 mM KCl, 2 mM CaCl2 and 10 mM MgCl2 (pH 7.4) (buffer A). The [3H] -SCH-
58261 (Dionisotti et al, 1997, Br J Pharmacol 121, 353; InM) binding assay was carried out in 96-well plates in the presence of 2.5 μg of membrane protein, 0.5 mg of Ysi-poly-1-lysine SPA beads and 0.1 U adenosine deaminase in a final volume of 200 μl of buffer A. Nonspecific binding was defined using xanthine amine congener (XAC; 2 μM). Compounds were tested at 10 concentrations from 10 μM - 0.3 nM. All assays were conducted in duplicate and repeated at least two times. Assay plates were incubated for lhour at room temperature before centrifugation and then bound ligand determined using a Packard Topcount scintillation counter. IC50 values were calculated using a non-linear curve fitting program and Ki values calculated using the Cheng-Prussoff equation.
The preferred compounds show a pKi > 7.5.
Figure imgf000016_0001
Figure imgf000017_0001
The compounds of formula I and the pharmaceutically acceptable salts ofthe compounds of formula I can be used as medicaments, e.g. in the form of pharmaceutical preparations. The pharmaceutical preparations can be administered orally, e.g. in the form of tablets, coated tablets, dragees, hard and soft gelatine capsules, solutions, emulsions or suspensions. The administration can, however, also be effected rectally, e.g. in the form of suppositories, parenterally, e.g. in the form of injection solutions.
The compounds of formula I can be processed with pharmaceutically inert, inorganic or organic carriers for the production of pharmaceutical preparations. Lactose, corn starch or derivatives thereof, talc, stearic acids or its salts and the like can be used, for example, as such carriers for tablets, coated tablets, dragees and hard gelatine capsules. Suitable carriers for soft gelatine capsules are, for example, vegetable oils, waxes, fats, semi-solid and liquid polyols and the like. Depending on the nature ofthe active substance no carriers are, however, usually required in the case of soft gelatine capsules. Suitable carriers for the production of solutions and syrups are, for example, water, polyols, glycerol, vegetable oil and the like. Suitable carriers for suppositories are, for example, natural or hardened oils, waxes, fats, semi-liquid or liquid polyols and the like.
The pharmaceutical preparations can, moreover, contain preservatives, solubilizers, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. They can also contain still other therapeutically valuable substances.
Medicaments containing a compound of formula I or a pharmaceutically acceptable salt thereof and a therapeutically inert carrier are also an object ofthe present invention, as is a process for their production, which comprises bringing one or more compounds of formula I and/or pharmaceutically acceptable acid addition salts and, if desired, one or more other therapeutically valuable substances into a galenical administration form together with one or more therapeutically inert carriers.
In accordance with the invention compounds of formula I as well as their pharmaceutically acceptable salts are useful in the control or prevention of illnesses based on the adenosine receptor antagonistic activity, such as Alzheimer's disease, Parkinson's disease, neuroprotection, schizophrenia, anxiety, pain, respiration deficits, depression, asthma, allergic responses, hypoxia, ischaemia, seizure and substance abuse. Furthermore, compounds ofthe present invention may be useful as sedatives, muscle relaxants, antipsychotics, antiepileptics, anticonvulsants and cardiaprotective agents and for the production of corresponding medicaments.
The most preferred indications in accordance with the present invention are those, which include disorders of the central nervous system, for example the treatment or prevention of certain depressive disorders, neuroprotection and Parkinson's disease.
The dosage can vary within wide limits and will, of course, have to be adjusted to the individual requirements in each particular case. In the case of oral administration the dosage for adults can vary from about 0.01 mg to about 1000 mg per day of a compound of general formula I or ofthe corresponding amount of a pharmaceutically acceptable salt thereof. The daily dosage may be administered as single dose or in divided doses and, in addition, the upper limit can also be exceeded when this is found to be indicated.
Tablet Formulation (Wet Granulation)
Item Ingredients mg/tablet
5 mg 25 100 mg 500 mg
1. Compound of formula I 5 25 100 500
2. Lactose Anhydrous DTG 125 105 30 150
3. Sta-Rx 1500 6 6 6 30
4. Microcrystalline Cellulose 30 30 30 150
5. Magnesium Stearate 1 1 1 1 Total 167 167 167 831
Manufacturing Procedure
1. Mix items 1, 2, 3 and 4 and granulate with purified water.
2. Dry the granules at 50°C.
3. Pass the granules through suitable milling equipment. 4. Add item 5 and mix for three minutes; compress on a suitable press. Capsule Formulation
Item Ingredients mg/capsule
5mg 25]mg 100 mg 500 mg
1. Compound of formula I 5 25 100 500
2. Hydrous Lactose 159 123 148 —
3. Corn Starch 25 35 40 70
4. Talc 10 15 10 25
5. Magnesium Stearate 1 2 2 5 Total 200 200 300 600
Manufacturing Procedure
1. Mix items 1, 2 and 3 in a suitable mixer for 30 minutes.
2. Add items 4 and 5 and mix for 3 minutes.
3. Fill into a suitable capsule.
The following preparation and examples illustrate the invention but are not intended to limit its scope.
Example 1
(lS,4S)-2-Oxa-5-aza-bicyclo[2.2.1]heptane-5-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide
To a solution of 4-methoxy-7-morpholin-4-yl-benzothiazol-2-ylamine (265 mg, 1.0 mmol) in dichloromethane (15 ml) is subsequently added pyridine (0.24 ml, 3.0 mmol) and phenyl chloroformate (0.15 ml, 1.2 mmol) and the resulting solution stirred for 45 min at ambient temperature. Then (15,4S)-2-oxa-5-aza-bicyclo[2.2.1]heptane (490 mg, 3.6 mmol) is added and the mixture stirred at ambient temperature for 15 min and at 40 °C for 2.5 h. After cooling to ambient temperature, saturated aqueous sodium carbonate (15 ml) is added, the organic phase is separated, dryed and the solvent evaporated in vacuo. Flash chromatography (silica, eluent: dichloromethane containing methanol (gradient from 0 to 5 %)) afforded the title compound as white crystals (135 mg, 35 % yield). MS: m/e=391(M+H+).
Following the general method of example 1 the compounds of examples 2 to 37 were prepared. Example 2
l-(4-Methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-3-(tetrahydro-pyran-4-yl)-urea Using tetrahydro-pyran-4-yl-amine, the title compound was prepared as white crystals in 62 % yield. MS: m/e=393(M+H+).
Example 3
3-en o-Hydroxy-8-aza-bicyclo [3.2.1 ] octane-8-carboxylic acid (4-methoxy-7-morpholin- 4-yl-benzothiazol-2-yl)-amide
Using 8-aza-bicyclo[3.2.1]octan-3-en<io-ol the title compound was prepared as white crystals in 49 % yield. MS: m/e=419(M+H+).
Example 4
2-Methyl- l-oxo-2,8-diaza-spiro [4.5] decane-8-carboxylic acid (4-mefhoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide
Using 4-spiro-[3-(N-methyl-2-pyrrolidinone)]piperidine, the title compound was prepared as white crystals in 43 % yield. MS: m/e=460(M+H+).
Example 5
l-Oxo-2,8-diaza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl- b enzothiazol-2-yl) -amide
Using 4-spiro- [3- (2-pyrrolidinone)] piperidine, the title compound was prepared as white crystals in 40 % yield. MS: m/e=446(M+H+).
Example 6
4-Isopropyl-piperazine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2- yl)-amide
Using l-(2-propyl)-piperazine, the title compound was prepared as white crystals in 62 % yield. MS: m/e=420(M+H+).
Example 7
4-Phenyl-piperazine- 1-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)- amide
Using 1-penyl-piperazine, the title compound was prepared as white crystals in 53 % yield. MS: m/e=454(M+H+). Example 8
4-Benzyl-4-hydroxymethyl-piperidine- 1-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide
Using (4-benzyl-piperidin-4-yl)-methanol, the title compound was prepared as light brown solid in 6 % yield. MS: m/e=497(M+H+).
Example 9 l-Cyclohexyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea Using Cyclohexyl-methyl-amine, the title compound was prepared as white crystals in 73 % yield. MS: m/e=405(M+H+). Example 10
3-Aza-spiro[5.5]undecane-3-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol- 2-yl)-amide
Using 3-aza-spiro[5.5]undecane, the title compound was prepared as white crystals in 38 % yield. MS: m/e=445(M+H+).
Example 11
8-Aza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2- yl)- amide
Using 8-aza-spiro[4.5]decane, the title compound was prepared as white crystals in 48 % yield. MS: m/e=431(M+H+).
Example 12
2-Aza-bicyclo [2.2.2] octane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol- 2-yl)-amide
Using 2-aza-bicyclo [2.2.2] octane, the title compound was prepared as white crystals in 47 % yield. MS: m/e=403(M+H+).
Example 13 l-Oxa-8-aza-spiro[4.5]decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl- b enzothiazol-2-yl) -amide
Using l-oxa-8-aza-spiro[4.5]decane, the title compound was prepared as white crystals in 40 % yield. MS: m/e=433(M+H+). Example 14
(JR)-4-(l-Hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide
Using (J?)-4-(l-hydroxy-ethyl)-piperidine, the title compound was prepared as white crystals in 21 % yield. MS: m/e= 421(M+H+).
Example 15
(5)-4-(l-Hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide
Using (S)-4-(l-hydroxy-ethyl)-piperidine, the title compound was prepared as white crystals in 53 % yield. MS: m/e= 421(M+H+).
Example 16
4- (Methanesulfonylamino-methyl)-piperidine- 1-carboxylic acid (4-methoxy-7- morpholin-4-yl-benzothiazol-2-yl)-amide
Using piperidin-4-ylmethyl-carbamic acid tert-butyl ester, [l-(4-methoxy-7-morpholin-4- yl-benzothiazol-2-ylcarbamoyl)-piperidin-4-ylmethyl]-carbamic acid tert-butyl ester was prepared as white solid. Subsequent deprotection with trifluoro acetic acid and reaction with methanesulfonyl chloride/pyridine under standard conditions afforded the title compound as white crystals in 44 % overall yield. MS: m/e= 482([M-H+]").
Example 17 Piperidine-l,4-dicarboxylic acid 4-amide 1- [(4-methoxy-7-morpholin-4-yl-benzothiazol- 2-yl)-amide]
Using piperidine-4-carboxylic acid amide, the title compound was prepared as white crystals in 44 % yield. MS: m/e= 420(M+H+).
Example 18 4- Methyl-3-oxo-piperazine- 1-carboxylic acid (4-methoxy-7-piperidin-l-yl-benzothiazol- 2-yl)-amide
Using 4-methoxy-7-piperidin-l-yl-benzothiazol-2-ylamine and 4-methyl-3-oxo- piperazine, the title compound was prepared as yellow solid in 84 % yield. MS: m/e= 404(M+H+). Example 19
l-Oxa-8-aza-spiro[4.5]decane-8-carboxylic acid (4-methoxy-7-piperidin-lyl- benzothiazol-2-yl)-amide
Using 4-methoxy-7-piperidin-l-yl-benzothiazol-2-ylamine and l-oxa-8-aza- spiro[4.5]decane, the title compound was prepared as beige crystals in 52 % yield. MS: m/e= 431(M+H+).
Example 20
4-Hydroxy-4-(4-methyl-benzyl)-piperidine- 1-carboxylic acid (4-chloro-7-piperidin-l-yl- benzothiazol-2-yl)-amide Using 4-chloro-7-piperidin-l-yl-benzothiazol-2-ylamine and 4-hydroxy-4-(4-methyl- benzyl)-piperidine, the title compound was prepared as white solid in 70 % yield. MS: m/e= 431(M+H+).
Example 21 l-(4-Chloro-7-piperidin-l-yl-benzothiazol-2-yl)-3-cyclohexyl-urea Using 4-chloro-7-piperidin-l-yl-benzothiazol-2-ylamine and cyclohexylamine, the title compound was prepared as white solid in 73 % yield. MS 394(M+H+).
Example 22
4-Benzyl-piperidine- 1-carboxylic acid (4-chloro-7-piperidin-l-yl-benzothiazol-2-yl)- amide Using 4-chloro-7-piperidin-l-yl-benzothiazol-2-ylamine and 4-benzylpiperidine, the title compound was prepared as white solid in 80 % yield. MS 470(M+H+).
Example 23
l-(4ds-Fluoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl- urea
Using ( 's)-(4-fluoro-cyclohexyl)-methyl-amine the title compound was prepared as white crystals (yield 24 %), mp 201-204°C. MS: m/e=423 (M+H+).
Example 24
l-(4,4-Difluoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea Using (4,4-difluoro-cyclohexyl)-methyl-amine the title compound was prepared as white crystals (yield 44 %), mp 189-192°C. MS: m/e=441(M+H+).
Example 25
(ds)-l-(4-Methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea
Using (αs)-(4-methoxy-cyclohexyl)-methyl-amine the title compound was prepared as white crystals (yield 39 %), mp 198-200 °C. MS: m/e=435 (M+H+).
Example 26
(lR)-l,8,8-Trimethyl-3-aza-bicyclo[3.2.1]octane-3-carboxylic acid (4-methoxy-7- morpholin-4-yl-benzothiazol-2-yl)-amide
Using camphidine the title compound was prepared as white crystals (yield 75 %), mp 185- 189°C. MS: m/e=445 (M+H+).
Example 27
(tr πs)-l-(4-Hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea
Using (trαπs)-(4-hydroxy-cyclohexyl)-methyl-amine the title compound was prepared as off-white solid (yield 44%), mp 158-162°C. MS: m/e=421 (M+H+).
Example 28
[ 1 ,4] Oxazepane-4-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)- amide
Using [l,4]oxazepane the title compound was prepared as light-yellow solid (yield 57%), mp 171-172°C. MS: m/e=393 (M+H+).
Example 29
( 's)-l-(4-Hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea
Using (czs)-(4-hydroxy-cyclohexyl)-methyl-amine the title compound was prepared as white solid (yield 66%), mp 169-171°C. MS: m/e=421 (M+H+). Example 30
2-Oxa-5-aza-bicyclo [2.2.2] octane-5-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide
Using 2-oxa-5-aza-bizyclo [2.2.2] octane the title compound was prepared as white solid (yield 69%), mp 164-170°C. MS: m/e=405 (M+H+).
Example 31
l,4-Diaza-bicyclo[3.2.1]octane-4-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide
Using l,4-diaza-bicyclo[3.2.1]octane the title compound was prepared as light-yellow crystals (yield 51 %). MS: m/e=404 (M+H+).
Example 32
(trans)-\ - (4-Methoxy-cyclohexyl)-3- (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)- 1- meth l-urea
Using (traπs)-(4-methoxy-cyclohexyl)-methyl-amine the title compound was prepared as white solid (yield 48 %), mp 211-213°C. MS: m/e=435 (M+H+).
Example 33
(lS,4R)-2-Aza-bicyclo[2.2.1]heptane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide
Using (lS,4R)-2-aza-bicyclo[2.2.1]heptane the title compound was prepared as white crystals (yield 67 %), mp 149 °C. MS: m/e=389 (M+H+).
Example 34
3 - (4-Methoxy- 7-morpholin-4-yl-benzothiazol-2-yl) - 1 -methyl- 1 - (tetrah dr o-pyran-4-yl)- urea
Using (4-tetrahydropyranyl)-methyl-amine the title compound was prepared as white solid (yield 56 %), mp 240-242 °C. MS: m/e=407 (M+H+).
Example 35
l-Cycloheptyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea Using cycloheptyl-methyl-amine the title compound was prepared as white solid (yield 70 %), mp 198-200 °C. MS: m/e=419 (M+H+).
Example 36
l-Cyclopentyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea
Using cyclopentyl-methyl-amine the title compound was prepared as white solid (yield 48 %), mp 110-125 °C. MS: m/e=391 (M+H+).
Example 37
l-Cyclopentyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-urea
Using cyclopentylamine the title compound was prepared as white crystals (yield 57 %), mp 191-194 °C. MS: m/e=377 (M+H+).
Preparation of intermediates for examples 1 to 22 Example 38
4-Benzyl-4-hydroxymethyl-piperidine
l,4-Dibenzyl-4-hydroxymethyl-piperidine (1.0 g, 3.4 mmol) in dichloromethane (20 ml) are treated with 1-chloroethyl-chloroformate (0.48 ml, 4.3 mmol, dissolved in 1.5 ml dichloromethane) and the resulting solution is stirred at 0°C for 30 min. The solvent is removed in vacuo and the resulting residue refluxed in methanol (20 ml) for 40 min. After removel ofthe volatile components in vacuo, the title compound is isolated by flash chromatography (silca, eluent dichloromethane/methanol/triethylamine (9:1:0.1, then 4:1:0.1 followed by 3:1:0.1)) as a brown resin in 40% yield. MS 206(M+H+).
Example 39
l,4-Dibenzyl-4-hydroxymethyl-piperidine
Was prepared from l,4-dibenzyl-piperidine-4-carboxylic acid ethyl ester (/. Chem. Soc, Perkin Trans. 1 1996, 20, 2545-2551.) by lithium aluminium hydride reduction in tetrahydrofurane under standard conditions in 81% yield. MS 296(M+H+).
Example 40
3 - Aza-spiro [5.5] undecane Was prepared from (3,3-tetramethylenglutarimide by lithium aluminium hydride reduction in tetrahydrofurane under standard conditions. Flash chromatography (silica, eluent dichloromethane/methanol/triethylamine 10:2:0.1) afforded the title compound as colorless oil (94% yield). MS 140(M+H+).
Example 41
8-Aza-spiro[4.5]decane
Was prepared from (3,3-pentamethylenglutarimide by lithium aluminium hydride reduction in tetrahydrofurane under standard conditions. Flash chromatography (silica, eluent dichloromethane/methanol/triethylamine 10:2:0.1) afforded the title compound as light yellow oil (>95% yield). MS 154(M+H+).
Example 42
(trøns)-(4-hydroxy-cyclohexyl)-methyl-amine
The title compound was prepared from (trans)-(4-hydroxy-cyclohexyl)-amine by reaction with di-tert. -butyl dicarbonate in aqueous sodium hydroxide under standard conditions and subsequent reduction with lithium aluminum hydride in THF under standard conditions.
If not described differently, the other N-methylated amines were prepared in the same manner.
Example 43
(ds)-(4-fluoro-cyclohexyl)-methyl-amine
The title compound was prepared from (ds)-(4-fluoro-cyclohexyl)-carbamic acid benzyl ester by lithium aluminum hydride reduction under standard conditions in 91 % yield.
Example 44
(d5)-(4-fluoro-cyclohexyl)-carbamic acid benzyl ester
(trøπs)-(4-hydroxy-cyclohexyl)-carbamic acid benzyl ester (900 mg, 3.6 mmol) are dissolved in dichloromethane (30 ml) and treated with diethylamino-sulfurtrifluoride (1 ml, 7.2 mmol). After 1 ha at room temperature, 5 % aqueous sodium hydrogen carbonate (15.3 g, 7.2 mmol) are added and stirring continued for another hour. The layers are separated, the aqueous phase is extracted twice with each 20 ml of dichloromethane, the combined organic layers are dried with magnesium sulfate and evaporated. Flash chromatography (silica, hexane containing 0 to 30 % ethyl acetate) afforded the title compound as light-yellow crystals (yield 14 %), mp 105-107°C . MS: m/e=252 (M+H+).
Example 45
(4,4-difluoro-cyclohexyl)-methyl-amine
The title compound was prepared from 4,4-difluoro-cyclohexanone (prepared from 8,8- Difluoro-l,4-dioxa-spiro[4.5]decane by deprotection with sulfuric acid under standard conditions) and methylamine by reductive amination under standard conditions (Pd hydroxide in methanol, 1 atm hydrogen) in ~50 % yield. Recrystallization ofthe hydrochloride from ethanol/diethylether afforded analytical pure material. Light-brown solid, mp 137-144 °C. MS: m/e=186 (M+H+).
Example 46
8,8-Difluoro-l,4-dioxa-spiro[4.5]decane
l,4-Dioxa-spiro[4.5]decan-8-one (9.0 g, 56 mmol) and (diethylamino)sulfur trifluoride (19 g, 112 mmol) are reacted in dichloromethane (180 ml) for 2h at room temperature. The mixture is poured in water (300 ml), the layers are separated and the aqueous phase back-extracted twice with dichloromethane (50 ml). The combined organic phases are dried with magnesium sulfate and evaporated. Distillation under reduced pressure over a vigreux-collumn afforded the title compound as colorless liquid (6.0 g, 60 %), bp 65-72°C at 13-14 mbar, MS: m/e=186 (M+), contaminated with -30 % 8-Fluoro-l,4-dioxa- spiro[4.5]dec-7-ene, MS: m/e=158 (M+).
Example 47
2-oxa-5-aza-bicyclo [2.2.2] octane
The title compound was prepared from 2-oxa-5-aza-bicyclo [2.2.2] octan-6-one (/. Polymer Sci. 1990, 28, 3251-60) by lithium aluminum hydride reduction under standard conditions in 84% yield. MS: m/e=113 (M+).
Example 48
1,4-Diaza-bicyclo [3.2.1] octane
Was prepared according to the procedure published in US3,954,766 (1976). MS: m/e=112
(M+). Example 49
(lS,4R)-2-Aza-bicvclo[2.2.11heptane
The title compound was prepared from (lS,4R)-2-aza-bicyclo[2.2.1]heptan-3-one by lithium aluminum hydride reduction under standard conditions in 88 % yield. MS: m/e=97 (M+).

Claims

Claims
1. The use of compounds ofthe general formula
Figure imgf000030_0001
wherein
R is lower alkoxy or halogen;
R R2 are independently from each other hydrogen, lower alkyl, cycloalkyl, or tetrahydropyran-4-yl, or R1 and R2 form together with the N atom to which they are attached heterocyclic rings, selected from the group consisting of 2-oxa-5-aza-bicyclo[2.2.1]heptane,
3-endo-hydroxy-8-aza-bicyclo [3.2.1 ] octane,
2-aza-bicyclo [2.2.2] octane, l-oxo-2,8-diaza-spiro[4.5]decane,
3-aza-spiro[5.5]undecane, 8-aza-spiro[4.5]decane, l-oxa-8-aza-spiro[4.5]decane,
1,8, 8-trimethyl-3-aza-bicyclo[3.2.1] octane,
[l,4]oxazepane,
2-oxa-5-aza-bicyclo [2.2.2] octane, 8-oxa-3-aza-bicyclo [3.2.1] octane,
1 ,4-diaza-bicyclo [3.2.1] octane,
2-aza-bicyclo[2.2.1]heptane,
3-aza-bicyclo[3.2.1] octane, which rings may be unsubstituted or substituted by lower alkyl, or is selected from piperazinyl, unsubstituted or mono or di-substituted by lower alkyl, phenyl or oxo, or is selected from piperidin-1-yl, substituted by -(CH2)n-NR'S(O)2-lower alkyl, -C(O)NR'2 or
-(CH2)n-phenyl, wherein the phenyl ring is unsubstituted or substituted by lower alkyl;
R' is hydrogen or lower alkyl, independently from each other in case R'2;
X is -O- or -CH2 and
n is O, 1, 2, 3 or 4 and pharmaceutically acceptable acid addition salts thereof for the manufacture of medicaments for the treatment of diseases, related to the adenosine A2 receptor system.
2. The use of compounds of formula I according to claim 1, wherein such diseases include Alzheimer's disease, Parkinson's disease, Huntington's disease, neuroprotection, schizophrenia, anxiety, pain, respiration deficits, depression, drug addiction, such as amphetamine, cocaine, opioids, ethanol, nicotine, cannabinoids, or asthma, allergic responses, hypoxia, ischaemia, seizure substance abuse, and they maybe useful as sedatives, muscle relaxants, antipsychotics, antiepileptics, anticonvulsants and cardiaprotective agents for disorders such as coronary artery disease and heart failure.
3. The use of compounds of formula I according to claims 1 or 2, wherein X is -O-.
4. The use of compounds of formula I according to claim 3, wherein the compound is
(lS,4S)-2-oxa-5-aza-bicyclo[2.2.1]heptane-5-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
3-eπdo-hydroxy-8-aza-bicyclo[3.2.1]octane-8-carboxylic aάd (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
2-methyl- l-oxo-2,8-diaza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
1 -oxo-2,8-diaza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide, 4-benzyl-4-hydroxymethyl-piperidine- 1-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
3-aza-spiro[5.5]undecane-3-carboxylic cid (4-methoxy-7-morpholin-4-yl-benzothiazol-
2-yl) -amide,
8-aza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2- yl)-amide,
2-aza-bicyclo [2.2.2] octane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-
2-yl) -amide,
1 -oxa-8-aza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide, (Λ)-4-(l-hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
(S)-4-(l-hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide, 4-(methanesulfonylamino-methyl)-piperidine-l-carboxylic acid (4-methoxy-7- morpholin-4-yl-benzothiazol-2-yl)-amide, piperidine- 1,4-dicarboxylic acid 4-amide l-[(4-methoxy-7-morpholin-4-yl-benzothiazol-
2-yl)-amide], l-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-3-(tetrahydro-pyran-4-yl)-urea, 4-isopropyl-piperazine- 1-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2- yl)-amide,
4-phenyl-piperazine- 1-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)- amide, l-cyclohexyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea, l-(4d5-fluoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl- urea, l-(4ds-fluoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl- urea,
(ds)-l-(4-methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
(tmπs)-l-(4-hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
[ 1,4] oxazepane-4-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)- amide, (ds)-l-(4-hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
2-oxa-5-aza-bicyclo[2.2.2]octane-5-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
(tmπs)-l-(4-methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
(lS,4R)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-l-(tetrahydro-pyran-4-yl)- urea, l-cycloheptyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea, l-cyclopentyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl-urea or l-cyclopentyl-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-urea.
5. The use of compounds of formula I according to claims 1 or 2, wherein X is -CH2-.
6. The use of compounds of formula I according to claim 5, which compounds are l-oxa-8-aza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-piperidin-lyl-benzothiazol- 2-yl) -amide,
4-hydroxy-4-(4-methyl-benzyl)-piperidine-l-carboxylic acid (4-chloro-7-piperidin-l-yl- benzothiazol-2-yl) -amide,
4-benzyl-piperidine- 1-carboxylic acid (4-chloro-7-piperidin-l-yl-benzothiazol-2-yl)- amide, 4-methyl-3-oxo-piperazine- 1-carboxylic acid (4-methoxy-7-piperidin-l-yl-benzothiazol- 2-yl) -amide or l-(4-chloro-7-piperidin-l-yl-benzothiazol-2-yl)-3-cyclohexyl-urea.
7. Compounds of formula
Figure imgf000033_0001
wherein
R is lower alkoxy or halogen;
R1 and R2 form together with the N atom to which they are attached heterocyclic rings, selected from the group consisting of 2-oxa-5-aza-bicyclo[2.2.1]heptane,
3-endo-hydroxy-8-aza-bicyclo [3.2.1] octane,
2-aza-bicyclo [2.2.2] octane, l-oxo-2,8-diaza-spiro[4.5]decane,
3-aza-spiro[5.5]undecane, 8-aza-spiro[4.5]decane,
1 -oxa-8-aza-spiro [4.5] decane, l,8,8-trimethyl-3-aza-bicyclo[3.2.1] octane,
[l,4]oxazepane, 2-oxa-5-aza-bicyclo [2.2.2] octane, 8-oxa-3-aza-bicyclo[3.2.1]octane, 1,4-diaza-bicyclo [3.2.1 ] octane, 2-aza-bicyclo [2.2.1] heptane, 3-aza-bicyclo[3.2.1]octane, which rings may be unsubstituted or substituted by lower alkyl, or is selected from piperidin-1-yl, substituted by-(CH2)n-NR'S(O)2-lower alkyl, -C(O)NR'2 or -(CH2)n-phenyl, wherein the phenyl ring is unsubstituted or substituted by lower alkyl;
R' is hydrogen or lower alkyl, independently from each other in case R'2;
X is -O- or CH2-; and
n is 0, 1, 2, 3 or 4 and pharmaceutically acceptable acid addition salts thereof.
8. Compounds of formula IA according to claim 7, wherein X is -O-.
9. Compounds of formula IA according to claim 8, which compounds are
(lS,4S)-2-oxa-5-aza-bicyclo[2.2.1]heptane-5-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
3-eπdo-hydroxy-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide,
2-methyl-l-oxo-2,8-diaza-spiro[4.5]decane-8-carboxylic acid (4-methoxy-7-morpholin-4- yl-benzothiazol-2-yl)-amide, l-oxo-2,8-diaza-sρiro[4.5]decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide, 4-benzyl-4-hydroxymethyl-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzofhiazol-2-yl)-amide,
3-aza-spiro[5.5]undecane-3-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-
2-yl) -amide,
8-aza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-2- yl) -amide,
2-aza-bicyclo [2.2.2] octane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl-benzothiazol-
2 -yl)- amide,
1 -oxa-8-aza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide, (#)-4-(l-hydroxy-ethyl)-piperidine-l-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
(5) -4- (1-hydroxy-ethyl) -piperidine- 1-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl)-amide,
4-(methanesulfonylamino-methyl)-piperidine- 1-carboxylic acid (4-methoxy-7- morpholin-4-yl-benzothiazol-2-yl)-amide, piperidine- 1,4-dicarboxylic acid 4-amide l-[(4-methoxy-7-morpholin-4-yl-benzothiazol-
2-yl)-amide],
(lR)-l,8,8-trimethyl-3-aza-bicyclo[3.2.1]octane-3-carboxylic acid (4-methoxy-7- morpholin-4-yl-benzothiazol-2-yl)-amide, 2-oxa-5-aza-bicyclo [2.2.2] octane-5-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide, l,4-diaza-bicyclo[3.2.1]octane-4-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzothiazol-2-yl) -amide or
(lS,4R)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid (4-methoxy-7-morpholin-4-yl- benzofhiazol-2-yl)-amide.
10. Compounds of formula IA according to claim 7, wherein X is -CH2-.
11. Compounds of formula IA according to claim 10, wherein the compound is
1 -oxa-8-aza-spiro [4.5] decane-8-carboxylic acid (4-methoxy-7-piperidin-lyl-benzothiazol- 2-yl) -amide, 4-hydroxy-4-(4-methyl-benzyl)-piperidine-l-carboxylic acid (4-chloro-7-piperidin-l-yl- benzothiazol-2-yl)-amide or
4-benzyl-piperidine- 1-carboxylic acid (4-chloro-7-piperidin-l-yl-benzothiazol-2-yl)- amide.
12. Compounds of formula
Figure imgf000035_0001
wherein
R is lower alkoxy or halogen;
R12 is lower alkyl and R22 is cycloalkyl, substituted by one or two substituents, wherein the substituents are selected from the group, consisting of halogen, lower alkoxy or hydroxy;
X is -O- or CH2-;
and pharmaceutically acceptable acid addition salts thereof.
13. Compounds of formula IB according to claim 12, wherein X is -O-.
14. Compounds of formula IB according to claim 13, wherein the compound is
l-(4ds-fluoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l-methyl- urea, l-(4,4-difiuoro-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
(ds)-l-(4-methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea,
(tr ns)-l-(4-hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea, (ds)-l-(4-hydroxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- me hyl-urea or
(tra77s)-l-(4-methoxy-cyclohexyl)-3-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-l- methyl-urea.
15. A process for preparing a compound of formula IA or IB as defined in claims 7 to 14, which processes comprise
a) reacting a compound of formula
Figure imgf000036_0001
with phenyl chloroformate and then with a compound of formula
HNRnR21 (3A) or HNR12R22 (3B)
to a compound of formula
Figure imgf000037_0001
wherein R and X are as defined in claim 1, and R and R form together with the N atom to which they are attached heterocyclic rings, selected from the group consisting of 2-oxa-5-aza-bicyclo[2.2.1]heptane, 3-endo-hydroxy-8-aza-bicyclo [3.2.1] octane, 2-aza-bicyclo [2.2.2] octane, l-oxo-2,8-diaza-spiro[4.5]decane, 3-aza-spiro[5.5]undecane, 8-aza-spiro[4.5]decane, l-oxa-8-aza-spiro[4.5]decane, l,8,8-trimethyl-3-aza- bicyclo [3.2.1 ] octane, [1,4] oxazepane, 2-oxa-5-aza-bicyclo [2.2.2] octane, 8-oxa-3-aza-bicyclo [3.2.1] octane, l,4-diaza-bicyclo[3.2.1] octane, 2-aza-bicyclo[2.2.1]heptane or 3-aza-bicyclo[3.2.1]octane, and which rings maybe unsubstituted or substituted by lower alkyl, or is selected from piperidin-1-yl, substituted by-(CH2)n-phenyl, -(CH2)n-NR'S(O)2-lower alkyl, -C(O)NR'2 or -(CH2)n-phenyl and wherein the phenyl ring is unsubstituted or substituted by lower alkyl and R' is hydrogen or lower alkyl, independently from each other in case R'2 and n is described above, and R12 is alkyl and R22 is cycloalkyl, substituted by one or two substituents, wherein the substituents are selected from the group, consisting of halogen, lower alkoxy or hydroxy; or
if desired, converting the compounds obtained into pharmaceutically acceptable acid addition salts.
16. A compound according to any one of claims 7 to 14, whenever prepared by a process as claimed in claim 15 or by an equivalent method.
17. A medicament containing one or more compounds as claimed in any one of claims 7 to 14 and pharmaceutically acceptable excipients.
18. A medicament according to claim 17 for the treatment of diseases related to the adenosine receptor.
19. The use of a compound in any one of claims 7 to 14 for the treatment of diseases.
20. The use of a compound in any one of claims 7 to 14 for the manufacture of corresponding medicaments for the treatment of diseases related to the adenosine A2A receptor.
1. The invention as hereinbefore described.
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RU2311905C2 (en) 2007-12-10
US7019001B2 (en) 2006-03-28
AU2002356626B2 (en) 2007-11-29
US20040229893A1 (en) 2004-11-18
GT200200266A (en) 2003-07-03

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