1,4-Diazacycloheptane derivatives for the treatment of...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C540S575000

Reexamination Certificate

active

06407093

ABSTRACT:

The present invention relates to chemical compounds, in particular 1,4-diazacycloheptanes, to processes for their preparation and to chemical intermediates useful in such processes. The present invention further relates to 1,4-diazacycloheptanes, to pharmaceutical compositions containing them and to their use in methods of therapeutic treatment of animals including man, in particular in the treatment of neurological disorders.
Neurological disorders, for which the present compounds are useful, include stroke, head trauma, transient cerebral ischemic attack, and chronic neurodegenerative disorders such as Alzheimer's disease, Parkinson's disease, diabetic neuropathy, amyotrophic lateral sclerosis, multiple sclerosis and AIDS-related dementia.
The compounds useful in the present invention are believed to act by binding with the [
3
H]-emopamil binding site. Emopamil has classically been thought of as a neuroprotective agent whose efficacy is most likely derived from actions at either voltage-sensitive calcium channels (VSCC) or 5-HT
2
receptors. An apparent paradox to this logic is that verapamil, although chemically and pharmacologically very similar to emopamil, is not neuroprotective. While the lack of neuroprotective efficacy by verapamil was initially explained by lack of CNS penetration, recent studies suggest other factors may be involved (Keith et al., Br. J. Pharmacol. 113: 379-384, 1994).
[
3
H]-Emopamil binding defines a unique high affinity site that is not related to VSCC, is found in the brain, but is most prevalent in the liver (Moebius et al., Mol. Pharmacol. 43: 139-148, 1993). Moebius et al. have termed this the “anti-ischemic” binding site on the basis of high affinity displacement by several chemically disparate neuroprotective agents. In liver, the [
3
H]-emopamil binding site is localized to the endoplasmic reticulum.
Neuroprotective compounds are known, for example emopamil and ifenprodil, that exhibit high affinity for the [
3
H]-emopamil binding site. However these are not selective inhibitors and exhibit activity either at neuronal VSCC, the polyamine site of the NMDA receptor (N-Methyl-D-aspartate) and/or the sigma-1 binding site. We have now found a class of compounds that show selective action at the [
3
H]-emopamil binding site that are neuroprotective in global and focal models of cerebral ischemia without acting directly at either VSCC or NMDA receptors, and consequently exhibit fewer associated side effects than are conventionally seen with either emopamil (hypotension) or ifenprodil (behavioural manifestations). Such compounds are especially useful in treating neurodegeneration resulting from ischemia, for example in Alzheimer's disease, vascular dementia, Parkinson's disease, Huntington's disease and AIDS-related dementia. In another aspect such compounds are especially useful in treating stroke as they provide neuronal protection by preventing neuronal death in the penumbra region surrounding the core infarct.
Accordingly the present invention provides a compound of the formula (I):
wherein:
R is hydrogen, C
1-10
alkyl, C
3-8
cycloalkyl, C
3-8
cycloalkylC
1-6
alkyl, phenylC
1-6
alkyl or phenyl;
R
1
is C
1-6
alkyl, C
2-6
alkenyl, C
1-6
alkoxy, halo, hydroxy, C
1-6
alkanoyl, haloC
1-6
alkyl, cyano or nitro;
m is 0, 1 or 2;
R
2
is C
1-6
alkyl;
n is 0, 1 or 2;
wherein any phenyl ring is optionally substituted
or a pharmaceutically acceptable salt or in vivo hydrolysable ester, amide or carbamate thereof.
Any phenyl ring in R may be optionally substituted, for example by up to five substituents, preferably up to three substituents which may be the same or different. Typical substituents include: hydroxy, C
1-6
alkoxy for example methoxy, mercapto, C
1-6
alkylthio for example methylthio, amino, C
1-6
alkylamino for example methylamino, di-(C
1-6
alkyl)amino for example dimethylamino, carboxy, carbamoyl, C
1-6
alkylcarbamoyl for example methylcarbamoyl, di-C
1-6
alkylcarbamoyl for example dimethylcarbamoyl, C
1-6
alkylsulphonyl for example methylsulphonyl, arylsulphonyl for example phenylsulphonyl, C
1-6
alkylaminosulphonyl for example methylaminosulphonyl, di-(C
1-6
alkyl)aminosulphonyl for example dimethylaminosulphonyl, nitro, cyano, cyano-C
1-6
alkyl for example cyanomethyl, hydroxyC
1-6
alkyl for example hydroxymethyl, amino-C
1-6
alkyl for example aminoethyl, C
1-6
alkanoylamino for example acetamido, C
1-6
alkoxycarbonylamino for example methoxycarbonylamino, C
1-6
alkanoyl for example acetyl, C
1-6
alkanoyloxy for example acetoxy, C
1-6
alkyl for example methyl, ethyl, isopropyl or tert-butyl, halo for example fluoro, chloro or bromo, trifluoromethyl or trifluoromethoxy.
In one aspect the present invention provides a compound of the formula (I) or a pharmaceutically acceptable salt or in vivo hydrolysable amide or carbamate thereof, wherein R is hydrogen, C
1-6
alkyl, C
3-8
cycloalkyl, C
3-8
cycloalkylC
1-6
alkyl, phenylC
1-6
alkyl or phenyl; R
1
is C
1-6
alkyl, C
1-6
alkoxy, halo, hydroxy, haloC
1-6
alkyl, cyano or nitro; m is 0, 1 or 2; R
2
is C
1-6
alkyl; and n is 0, 1 or 2; wherein any phenyl ring is optionally substituted.
Suitably R is hydrogen; C
1-10
alkyl for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, pentyl or 2-ethylheptyl. C
3-8
cycloalkyl for example cyclopropyl, cyclobutyl or cyclopentyl; C
3-8
cycloalkylC
1-6
alkyl for example cyclopropylmethyl, cyclobutylmethyl or cyclopentylmethyl; phenylC
1-6
alkyl for example benzyl, 2-phenethyl or 3-phenylpropyl.
Favourably R is hydrogen; C
1-6
alkyl for example methyl, ethyl, isopropyl, n-propyl, n-butyl, isobutyl, n-pentyl or 2-methylbutyl; or benzyl. More particularly R is methyl, ethyl, n-propyl, n-butyl or n-pentyl.
Suitably R
1
is C
1-6
alkyl for example methyl, ethyl or propyl; C
2-6
alkenyl for example vinyl; C
1-6
alkoxy for example methoxy, ethoxy or propoxy; halo for example bromo, chloro or fluoro; hydroxy; C
1-6
alkanoyl for example formyl or acetyl; haloC
1-6
alkyl for example trifluoromethyl; cyano or nitro.
Preferably R
1
is C
1-6
alkoxy for example methoxy or ethoxy or is halo for example bromo, chloro or fluoro. In a particularly preferred aspect, m is one and R
1
is methoxy, for example at the 6-position or the 8-position of the 3,4-dihydro-2H-benzothiopyran-4-yl ring system, most preferably at the 8-position. In another particularly preferred aspect, m is one and R
1
is bromo or fluoro, for example at the 6-position of the 3,4-dihydro-2H-benzothiopyran-4-yl ring system.
In another particularly preferred aspect m is zero.
Suitably R
2
is C
1-6
alkyl for example methyl or ethyl.
In a preferred aspect n is zero.
A particular class of preferred compounds is that of the formula (II):
wherein R
3
is hydrogen, C
1-6
alkyl or benzyl, and R
4
is hydrogen, C
1-6
alkoxy or C
1-6
alkyl.
Particular compounds of the present invention include those of the Examples hereinafter and N-methyl-N′-(3,4-dihydro-6-fluoro-2H-benzothiopyran-4-yl)homopiperazine.
The compounds of the present invention possess a chiral centre at the 4-position of the 3,4-dihydro-2H-benzothiopyran-4-yl ring system (that is the carbon atom to which the nitrogen containing ring is attached). Other chiral centres may be present when n is one or two and in any of the substituents R—R
4
.
The present invention covers all enantiomers, diastereoisomers and mixtures thereof that inhibit the [
3
H]-emopamil binding site.
As mentioned hereinabove, the compounds of the present invention possess a chiral centre at the 4-position of the 3,4-dihydro-2H-benzothiopyran-4-yl ring system. It is preferred that this centre has the S-stereochemistry under the Cahn-Prelog-Ingold sequence rules. It is preferred that any R or S-enantiomer is substantially free of the corresponding S or R-enantiomer, suitably 90%, more suitably 95%, and for example 96%, 97%, 98% or 99% free of the other enantiomer.
Suitable pharmaceutically acceptable salts include acid addition salts such as hydrochloride, hydrobromide, citrate and

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

1,4-Diazacycloheptane derivatives for the treatment of... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with 1,4-Diazacycloheptane derivatives for the treatment of..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and 1,4-Diazacycloheptane derivatives for the treatment of... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2974934

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.