U.S. patent application number 11/526591 was filed with the patent office on 2009-03-12 for n-formyl hydroxylamine derivatives as inhibitors of bacterial polypeptide formylase for treating microbial infections.
This patent application is currently assigned to British Biotech Pharmaceuticals Ltd.. Invention is credited to Paul Raymond Beckett, Steven Launchbury, Gilles Pain, Lisa Marie Pratt.
Application Number | 20090069322 11/526591 |
Document ID | / |
Family ID | 26245320 |
Filed Date | 2009-03-12 |
United States Patent
Application |
20090069322 |
Kind Code |
A1 |
Beckett; Paul Raymond ; et
al. |
March 12, 2009 |
N-FORMYL HYDROXYLAMINE DERIVATIVES AS INHIBITORS OF BACTERIAL
POLYPEPTIDE FORMYLASE FOR TREATING MICROBIAL INFECTIONS
Abstract
Compounds of formula (I) are antibacterial or antiprotozoal
agents for treatment of infections in humans and non-human mammals,
wherein: Z represents a radical of formula --N(OH)CH(.dbd.O) or
formula C(.dbd.O)NH(OH); R.sub.1 represents hydrogen, methyl or
trifluoromethyl, or except when Z is a radical of formula
--N(OH)CH(.dbd.O), a hydroxy, halo or amino group; R.sub.2
represents a group R.sub.10--(X).sub.n-(ALK).sub.m-- wherein
R.sup.10, ALK, X, m and n are as defined in the specification;
R.sup.3 represents hydrogen, (C.sub.1-C.sub.6) alkyl or
phenyl(C.sub.1-C.sub.6)alkyl-; and R.sub.5 and R.sub.6 are as
defined in the specification. ##STR00001##
Inventors: |
Beckett; Paul Raymond;
(Oxford, GB) ; Launchbury; Steven; (Oxford,
GB) ; Pain; Gilles; (Oxford, GB) ; Pratt; Lisa
Marie; (Oxford, GB) |
Correspondence
Address: |
BANNER & WITCOFF, LTD.
1100 13th STREET, N.W., SUITE 1200
WASHINGTON
DC
20005-4051
US
|
Assignee: |
British Biotech Pharmaceuticals
Ltd.
Oxford
GB
|
Family ID: |
26245320 |
Appl. No.: |
11/526591 |
Filed: |
September 26, 2006 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10432252 |
Nov 10, 2003 |
7173053 |
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PCT/GB01/04965 |
Nov 8, 2001 |
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11526591 |
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Current U.S.
Class: |
514/235.5 ;
514/254.05; 514/326; 514/341; 514/365; 514/397; 514/400; 544/139;
544/370; 546/210; 546/272.7; 548/203; 548/311.1; 548/335.5 |
Current CPC
Class: |
A61K 31/417 20130101;
Y02A 50/30 20180101; A61P 33/02 20180101; C07D 233/64 20130101;
A61P 31/04 20180101; Y02A 50/411 20180101; C07D 235/14
20130101 |
Class at
Publication: |
514/235.5 ;
514/400; 514/397; 514/341; 514/326; 514/254.05; 514/365; 544/139;
546/210; 544/370; 546/272.7; 548/203; 548/311.1; 548/335.5 |
International
Class: |
A61K 31/5377 20060101
A61K031/5377; A61K 31/496 20060101 A61K031/496; A61K 31/454
20060101 A61K031/454; A61K 31/4439 20060101 A61K031/4439; A61K
31/426 20060101 A61K031/426; A61K 31/4166 20060101 A61K031/4166;
C07D 403/02 20060101 C07D403/02; C07D 413/02 20060101 C07D413/02;
C07D 417/02 20060101 C07D417/02 |
Foreign Application Data
Date |
Code |
Application Number |
Nov 23, 2000 |
GB |
0028519.7 |
Jul 11, 2001 |
GB |
0116864.0 |
Claims
1-16. (canceled)
17. A method for the treatment of bacterial or protozoal infections
in humans and non-human mammals, which comprises administering to a
subject suffering such infection an antibacterially or
antiprotozoally effective dose of a compound of formula (I) or a
pharmaceutically or veterinarily acceptable salt, hydrate or
solvate thereof: ##STR00022## wherein: Z represents a radical of
formula --N(OH)CH(.dbd.O) or formula --C(.dbd.O)NH(OH); R.sub.1
represents hydrogen, methyl or trifluoromethyl, or, except when Z
is a radical of formula --N(OH)CH(.dbd.O), a hydroxy, halo or amino
group; R.sub.2 represents a group R.sub.10--(X).sub.n-(ALK).sub.m--
wherein R.sub.10 represents hydrogen, or a C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, aryl,
or heterocyclyl group, any of which may be unsubstituted or
substituted by (C.sub.1-C.sub.6)alkyl, (C.sub.1-C.sub.6)alkoxy,
hydroxy, mercapto, (C.sub.1-C.sub.6)alkylthio, amino, halo
(including fluoro, chloro, bromo and iodo), trifluoromethyl, cyano,
nitro, oxo, --COOH, --CONH.sub.2, --COOR.sup.A, --NHCOR.sup.A,
--CONHR.sup.A, --NHR.sup.A, --NR.sup.AR.sup.B, or
--CONR.sup.AR.sup.B wherein R.sup.A and R.sup.B are independently a
(C.sub.1-C.sub.6)alkyl group and ALK represents a straight or
branched divalent C.sub.1-C.sub.6 alkylene, C.sub.2-C.sub.6
alkenylene, or C.sub.2-C.sub.6 alkynylene radical, and may be
interrupted by one or more non-adjacent --NH--, --O-- or --S--
linkages, X represents --NH--, --O-- or --S--, and m and n are
independently 0 or 1; R.sub.3 represents the characterizing group
of a natural .alpha.-amino acid in which any functional group may
be protected, any amino group may be acylated and any carboxyl
group present may be amidated; or a group [Alk].sub.nR.sub.9 where
Alk is a (C.sub.1-C.sub.6)alkylene or (C.sub.2-C.sub.6)alkenylene
group optionally interrupted by one or more --O--, or --S--, atoms
or --N(R.sub.12)-- groups, where R.sub.12 is a hydrogen atom or a
(C.sub.1-C.sub.6)alkyl group, n is 0 or 1, and R.sub.9 is hydrogen
or an optionally substituted phenyl, aryl, heterocyclyl, cycloalkyl
or cycloalkenyl group or (only when n is 1) R.sub.9 may
additionally be hydroxy, mercapto, (C.sub.1-C.sub.6)alkylthio,
amino, halo, trifluoromethyl, nitro, --COOH, --CONH.sub.2,
--COOR.sup.A, --NHCOR.sup.A, --CONHR.sup.A, --NHR.sup.A,
--NR.sup.AR.sup.B, or --CONR.sup.AR.sup.B wherein R.sup.A and
R.sup.B are independently a (C.sub.1-C.sub.6)alkyl group; or a
benzyl group substituted in the phenyl ring by a group of formula
--OCH.sub.2COR.sub.8 where R.sub.8 is hydroxyl, amino,
(C.sub.1-C.sub.6)alkoxy, phenyl(C.sub.1-C.sub.6)alkoxy,
(C.sub.1-C.sub.6)alkylamino, di((C.sub.1-C.sub.6)alkyl)amino,
phenyl(C.sub.1-C.sub.6)alkylamino; or a
heterocyclic(C.sub.1-C.sub.6)alkyl group, either being
unsubstituted or mono- or di-substituted in the heterocyclic ring
with halo, nitro, carboxy, (C.sub.1-C.sub.6)alkoxy, cyano
(C.sub.1-C.sub.6)alkanoyl, trifluoromethyl (C.sub.1-C.sub.6)alkyl,
hydroxy, formyl, amino, (C.sub.1-C.sub.6)alkylamino,
di-(C.sub.1-C.sub.6)alkylamino, mercapto,
(C.sub.1-C.sub.6)alkylthio, hydroxy(C.sub.1-C.sub.6)alkyl,
mercapto(C.sub.1-C.sub.6)alkyl or
(C.sub.1-C.sub.6)alkylphenylmethyl; or a group
--CR.sub.aR.sub.bR.sub.c in which: each of R.sub.a, R.sub.b and
R.sub.c is independently hydrogen, (C.sub.1-C.sub.6)alkyl,
(C.sub.2-C.sub.6)alkenyl, (C.sub.2-C.sub.6)alkynyl,
phenyl(C.sub.1-C.sub.6)alkyl, (C.sub.3-C.sub.8)cycloalkyl; or
R.sub.c is hydrogen and R.sub.a and R.sub.b are independently
phenyl or heteroaryl such as pyridyl; or R.sub.c is hydrogen,
(C.sub.1-C.sub.6)alkyl, (C.sub.2-C.sub.6)alkenyl,
(C.sub.2-C.sub.6)alkynyl, phenyl(C.sub.1-C.sub.6)alkyl, or
(C.sub.3-C.sub.8)cycloalkyl, and R.sub.a and R.sub.b together with
the carbon atom to which they are attached form a 3 to 8 membered
cycloalkyl or a 5- to 6-membered heterocyclic ring; or R.sub.a,
R.sub.b and R.sub.c together with the carbon atom to which they are
attached form a Tricyclic ring (for example adamantyl); or R.sub.a
and R.sub.b are each independently (C.sub.1-C.sub.6)alkyl,
(C.sub.2-C.sub.6)alkenyl, (C.sub.2-C.sub.6)alkynyl,
phenyl(C.sub.1-C.sub.6)alkyl, or a group as defined for R.sub.c
below other than hydrogen, or R.sub.a and R.sub.b together with the
carbon atom to which they are attached form a cycloalkyl or
heterocyclic ring, and R.sub.c is hydrogen, --OH, --SH, halogen,
--CN, --CO.sub.2H, (C.sub.1-C.sub.4)perfluoroalkyl, --CH.sub.2OH,
--CO.sub.2(C.sub.1-C.sub.6)alkyl, --O(C.sub.1-C.sub.6)alkyl,
--O(C.sub.2-C.sub.6)alkenyl, --S(C.sub.1-C.sub.6)alkyl,
--SO(C.sub.1-C.sub.6)alkyl, --SO.sub.2(C.sub.1-C.sub.6)alkyl,
--S(C.sub.2-C.sub.6)alkenyl, --SO(C.sub.2-C.sub.6)alkenyl,
--SO.sub.2(C.sub.2-C.sub.6)alkenyl or a group -Q-W wherein Q
represents a bond or --O--, --S--, --SO-- or --SO.sub.2-- and W
represents a phenyl, phenylalkyl, (C.sub.3-C.sub.8)cycloalkyl,
(C.sub.3-C.sub.8)cycloalkylalkyl, (C.sub.4-C.sub.8)cycloalkenyl,
(C.sub.4-C.sub.8)cycloalkenylalkyl, heteroaryl or heteroarylalkyl
group, which group W may optionally be substituted by one or more
substituents independently selected from, hydroxyl, halogen, --CN,
--CO.sub.2H, --CO.sub.2(C.sub.1-C.sub.6)alkyl, --CONH.sub.2,
--CONH(C.sub.1-C.sub.6)alkyl, --CONH(C.sub.1-C.sub.6alkyl).sub.2,
--CHO, --CH.sub.2OH, (C.sub.1-C.sub.4)perfluoroalkyl,
--O(C.sub.1-C.sub.6)alkyl, --S(C.sub.1-C.sub.6)alkyl,
--SO(C.sub.1-C.sub.6)alkyl, --SO(C.sub.1-C.sub.6)alkyl, --NO.sub.2,
--NH.sub.2, --NH(C.sub.1-C.sub.6)alkyl,
--N((C.sub.1-C.sub.6)alkyl).sub.2, --NHCO(C.sub.1-C.sub.6)alkyl,
(C.sub.1-C.sub.6)alkyl, (C.sub.2-C.sub.6)alkenyl,
(C.sub.2-C.sub.6)alkynyl, (C.sub.3-C.sub.8)cycloalkyl,
(C.sub.4-C.sub.8)cycloalkenyl, phenyl or benzyl; and R.sub.4
represents hydrogen, (C.sub.1-C.sub.6)alkyl or
phenyl(C.sub.1-C.sub.6)alkyl-; and (a) R.sub.5 and R.sub.6
independently represent: hydrogen, halogen, trifluoromethyl, or
(C.sub.1-C.sub.6)alkyl, (C.sub.2-C.sub.6)alkenyl,
(C.sub.2-C.sub.6)alkynyl, aryl, heterocyclyl,
aryl(C.sub.1-C.sub.6)alkyl-, or
heterocyclyl(C.sub.1-C.sub.6)alkyl-, any of which may be optionally
substituted by (C.sub.1-C.sub.6)alkyl, halogen, trifluoromethyl,
cyano, nitro, oxo, phenoxy or phenylthio-, --OR.sup.A, --SR.sup.A,
--NHR.sup.A, --NR.sup.AR.sup.B, --NHCOR.sup.A--CONHR.sup.A,
--CONR.sup.AR.sup.B, or --COOR.sup.A, wherein R.sup.A and R.sup.B
are independently hydrogen or (C.sub.1-C.sub.4)alkyl, or in the
case where R.sup.A and R.sup.B are attached to a nitrogen atom then
R.sup.A and R.sup.B taken together with the nitrogen atom to which
they are attached form a monocyclic 5-7 membered ring; or (b)
R.sub.5 and R.sub.6 taken together with the carbon atoms to which
they are attached form a fused monocyclic or bicyclic carbocyclic
or heterocyclic ring which may be further substituted with any of
the substituent groups listed under (a).
18. A method as claimed in claim 17 wherein R.sub.2 is: optionally
substituted C.sub.1-C.sub.8 alkyl, C.sub.3-C.sub.6 alkenyl,
C.sub.3-C.sub.6 alkynyl or cycloalkyl; phenyl(C.sub.1-C.sub.6
alkyl)-, phenyl(C.sub.3-C.sub.6 alkenyl)- or phenyl(C.sub.3-C.sub.6
alkynyl)- optionally substituted in the phenyl ring;
cycloalkyl(C.sub.1-C.sub.6 alkyl)-, cycloalkyl(C.sub.3-C.sub.6
alkenyl)- or cycloalkyl(C.sub.3-C.sub.6 alkynyl)-optionally
substituted in the cycloalkyl ring; heterocyclyl(C.sub.1-C.sub.6
alkyl)-, heterocyclyl(C.sub.3-C.sub.6 alkenyl)- or
heterocyclyl(C.sub.3-C.sub.6 alkynyl)-optionally substituted in the
heterocyclyl ring; or
CH.sub.3(CH.sub.2).sub.p--O--(CH.sub.2).sub.q-- or
CH.sub.3(CH.sub.2).sub.pS(CH.sub.2).sub.q--, wherein p is 0, 1, 2
or 3 and q is 1, 2 or 3.
19. A method as claimed in claim 17 wherein R.sub.2 is methyl,
ethyl, n- or iso-propyl, n- and iso-butyl, n-pentyl, iso-pentyl,
3-methyl-but-1-yl, n-hexyl, n-heptyl, n-acetyl, n-octyl,
methylsulfanylethyl, ethylsulfanylmethyl, 2-methoxyethyl,
2-ethoxyethyl, 2-ethoxymethyl, 3-hydroxypropyl, allyl,
3-phenylprop-3-en-1-yl, prop-2-yn-1-yl, 3-phenylprop-2-yn-1-yl,
3-(2-chlorophenyl)prop-2-yn-1-yl, but-2-yn-1-yl, cyclopentyl,
cyclohexyl, cyclopentylmethyl, cyclopentylethyl, cyclopentylpropyl,
cyclohexylmethyl, cyclohexylethyl, cyclohexylpropyl,
furan-2-ylmethyl, furan-3-methyl, tetrahydrofuran-2-ylmethyl,
tetrahydrofuran-2-ylmethyl, phenylpropyl, 4-chlorophenylpropyl,
4-methylphenylpropyl, 4-methoxyphenylpropyl, benzyl,
4-chlorobenzyl, 4-methylbenzyl, or 4-methoxybenzyl.
20. A method as claimed in claim 17 wherein R.sub.2 is n-propyl,
n-butyl, n-pentyl, or cyclopentylmethyl.
21. (canceled)
22. A method as claimed in claim 17 wherein R.sub.3 is methyl,
ethyl, benzyl, 4-chlorobenzyl, 4-hydroxybenzyl, phenyl, cyclohexyl,
cyclohexylmethyl, pyridin-3-ylmethyl, tert-butoxymethyl,
naphthylmethyl, iso-butyl, sec-butyl, tert-butyl,
1-benzylthio-1-methylethyl, 1-methylthio-1-methylethyl,
1-mercapto-1-methylethyl, 1-methoxy-1-methylethyl,
1-hydroxy-1-methylethyl, 1-fluoro-1-methylethyl, hydroxymethyl,
2-hydroxethyl, 2-carboxyethyl, 2-methylcarbamoylethyl,
2-carbamoylethyl, or 4-aminobutyl.
23. A method as claimed in claim 17 wherein R.sub.3 is
tert-butyl.
24. A method as claimed in claim 17 wherein R.sub.4 is hydrogen or
methyl.
25. A method as claimed in claim 17 wherein R.sub.5 and R.sub.6 are
independently hydrogen, methyl, trifluoromethyl, phenyl, bromo,
chloro, fluoro, methoxy, hydroxymethyl, dimethylaminomethyl-,
ethoxymethyl-, 4-methyl-piperazine-1-carbonyl-,
4-methyl-piperazin-1-ylmethyl-, morpholin-4-ylmethyl-,
methoxycarbonyl, thiazol-2-yl-, phenoxymethyl-,
pyrrolidin-1-ylmethyl-, piperidin-1-ylmethyl-, --C(O)NH.sub.2,
(CH.sub.2).sub.2CO.sub.2CH.sub.3, --CH(OH)CH(CH.sub.3).sub.2,
--CH(OH)CH.sub.3, or --CH(OH)Ph; or wherein R.sub.5 and R.sub.6
taken together with the carbon atoms to which they are attached
form a fused benzo, naphtho or pyrido ring, which may be
substituted.
26. A method as claimed in claim 25 wherein R.sub.1 is hydrogen,
R.sub.2 is n-propyl, n-butyl, n-pentyl, or cyclopentylmethyl,
R.sub.3 is tert-butyl, and R.sub.4 is hydrogen or methyl.
Description
[0001] This invention relates to the use of hydroxamic acid and
N-formyl hydroxylamine derivatives as antibacterial and
antiprotozoal agents, to novel compounds within those classes, and
to pharmaceutical and veterinary compositions comprising such
compounds.
BACKGROUND TO THE INVENTION
[0002] In general, bacterial pathogens are classified as either
Gram-positive or Gram-negative. Many antibacterial agents
(including antibiotics) are specific against one or other
Gram-class of pathogens. Antibacterial agents effective against
both Gram-positive and Gram-negative pathogens are therefore
generally regarded as having broad spectrum activity.
[0003] Many classes of antibacterial agents are known, including
the penicillins and cephalosporins, tetracyclines, sulfonamides,
monobactams, fluoroquinolones and quinolones, aminoglycosides,
glycopeptides, macrolides, polymyxins, lincosamides, trimethoprim
and chloramphenicol. The fundamental mechanisms of action of these
antibacterial classes vary.
[0004] Bacterial resistance to many known antibacterials is a
growing problem. Accordingly there is a continuing need in the art
for alternative antibacterial agents, especially those which have
mechanisms of action fundamentally different from the known
classes.
[0005] Amongst the Gram-positive pathogens, such as Staphylococci,
Streptococci, Mycobacteria and Enterococci, resistant strains have
evolved/arisen which makes them particularly difficult to
eradicate. Examples of such strains are methicillin resistant
Staphylococcus aureus (MRSA), methicillin resistant coagulase
negative Staphylococci (MRCNS), penicillin, quinolone or macrolide
resistant Streptococcus pneumoniae and multiply resistant
Enterococcus faecium.
[0006] Pathogenic bacteria are often resistant to the
aminoglycoside, .beta.-lactam (penicillins and cephalosporins),
macrolide, quinolone and chloramphenicol types of antibiotic. The
mechanism of resistance can involve the enzymatic inactivation of
the antibiotic by hydrolysis, formation of inactive derivatives,
mutation of the molecular target and/or activation of transport
pumps. The .beta.-lactam (penicillin and cephalosporin) family of
antibiotics are characterised by the presence of a .beta.-lactam
ring structure. Resistance to this family of antibiotics in
clinical isolates is most commonly due to the production of a
"penicillinase" (.beta.-lactamase) enzyme by the resistant
bacterium which hydrolyses the .beta.-lactam ring thus eliminating
its antibacterial activity.
[0007] Recently there has been an emergence of vancomycin-resistant
strains of enterococci (Woodford N. 1998 Glycopeptide-resistant
enterococci: a decade of experience. Journal of Medical
Microbiology. 47(10):849-62). Vancomycin-resistant enterococci are
particularly hazardous in that they are frequent causes of hospital
based infections and are inherently resistant to most antibiotics.
Vancomycin works by binding to the terminal D-Ala-D-Ala residues of
the cell wall peptidoglycan precursor. The high-level resistance to
vancomycin is known as VanA and is conferred by genes located on a
transposable element which alter the terminal residues to
D-Ala-D-lac thus reducing the affinity for vancomycin.
[0008] In view of the rapid emergence of multidrug-resistant
bacteria, the development of antibacterial agents with novel modes
of action that are effective against the growing number of
resistant bacteria, particularly the vancomycin resistant
enterococci and .beta.-lactam antibiotic-resistant bacteria, such
as methicillin-resistant Staphylococcus aureus, is of utmost
importance.
BRIEF DESCRIPTION OF THE INVENTION
[0009] This invention is based on the finding that certain
hydroxamic acid and N-formyl hydroxylamine derivatives having
imidazole substituents have antibacterial and antiprotozoal
activity, and makes available new antibacterial and antiprotozoal
agents. The compounds with which this invention is concerned are
antibacterial with respect to a range of Gram-positive and
Gram-negative organisms.
[0010] Although it may be of interest to establish the mechanism of
action of the compounds with which the invention is concerned, it
is their ability to inhibit bacterial growth that makes them
useful. However, it is presently believed that their antibacterial
activity is due, at least in part, to intracellular inhibition of
bacterial polypeptide deformylase (PDF; EC 3.5.1.31).
[0011] All ribosome-mediated synthesis of proteins starts with a
methionine residue. In prokaryotes, the methionyl moiety carried by
the initiator tRNA is N-formylated prior to its incorporation into
a polypeptide. Consequently, N-formylmethionine is always present
at the N-terminus of a nascent bacterial polypeptide. However, most
mature proteins do not retain the N-formyl group or the terminal
methionine residue. Deformylation is required prior to methionine
removal, since methionine aminopeptidase does not recognise
peptides with an N-terminal formylmethionine residue (Solbiati et
al., J. Mol. Biol. 290:607-614, 1999). Deformylation is, therefore,
a crucial step in bacterial protein biosynthesis and the enzyme
responsible, PDF, is essential for normal bacterial growth.
Although the gene encoding PDF (def) is present in all pathogenic
bacteria for which sequences are known (Meinnel et al., J. Mol.
Biol, 266:939-49, 1997), it has no known eukaryotic counterpart,
making it an attractive target for antibacterial chemotherapy (for
a review see Giglione et al., Mol Microbiol., 36: 1197-1205,
2000).
[0012] The isolation and characterisation of PDF has been
facilitated by an understanding of the importance of the metal ion
in the active site (Groche et al., Biophys. Biochem. Res. Commun.,
246:324-6, 1998). The Fe.sup.2+ form is highly active in vivo but
is unstable when isolated due to oxidative degradation (Rajagopalan
et al., J. Biol. Chem. 273:22305-10, 1998). The Ni.sup.2+ form of
the enzyme has specific activity comparable with the ferrous enzyme
but is oxygen-insensitive (Ragusa et al., J. Mol. Biol. 1998,
280:515-23, 1998). The Zn.sup.2+ enzyme is also stable but is
almost devoid of catalytic activity (Rajagopalan et al., J. Am.
Chem. Soc. 119:12418-12419, 1997).
[0013] Several X-ray crystal structures and NMR structures of E.
coli PDF, with or without bound inhibitors, have been published
(Chan et al., Biochemistry 36:13904-9, 1997; Becker et al., Nature
Struct. Biol. 5:1053-8, 1998; Becker et al., J. Biol. Chem.
273:11413-6, 1998; Hao et al., Biochemistry, 38:4712-9, 1999;
Dardel et al., J. Mol. Biol. 280:501-13, 1998; O'Connell et al., J.
Biomol. NMR, 13:311-24, 1999), indicating similarities in active
site geometry to metalloproteinases such as thermolysin and the
metzincins.
[0014] The substrate specificity of PDF has been extensively
studied (Ragusa et al., J. Mol. Biol. 289:1445-57, 1999; Hu et al.,
Biochemistry 38:643-50, 1999; Meinnel et al., Biochemistry,
38:4287-95, 1999). These authors conclude that an unbranched
hydrophobic chain is preferred at P1', while a wide variety of P2'
substituents are acceptable and an aromatic amide substituent may
be advantageous at the P3' position. There have also been reports
that small peptidic compounds containing an H-phosphonate (Hu et
al., Bioorg. Med. Chem. Lett., 8:2479-82, 1998) or thiol (Meinnel
et al., Biochemistry, 38:4287-95, 1999; Huntingdon et al.,
Biochemistry, 39: 4543-51, 2000; Wei et al, J. Combinatorial Chem.,
2: 650-57, 2000) metal binding group are micromolar inhibitors of
PDF. Peptide aldehydes such as calpeptin (N-Cbz-Leu-norleucinal)
have also been shown to inhibit PDF (Durand et al., Arch. Biochem.
Biophys., 367:297-302, 1999). Recently, the naturally occurring
hydroxamic acid antibiotic actinonin, for which the target of its
antibacterial activity was previously unknown, was shown to be a
potent inhibitor of polypeptide deformylase (WO 99/39704, and Chen
et al, Biochemistry, 39: 1256-62, 2000). Examples of non-peptidic
PDF inhibitors with a carboxylic acid (Green et al., Arch. Biochem.
Biophys. 375: 355-8, 2000; Jayasekera et al., ibid., 381:313-6,
2000) or hydroxamic acid (Apfel et al., J. Med. Chem., 43: 2324-31,
2000) metal binding groups are also known.
[0015] It has been reported that PDF is present in eukaryotic
parasites such as Plasmodium falciparum (Meinnel, Parasitology
Today, 16: 165-8, 2000). Those authors also found evidence for the
presence of PDF in other parasites of humans, such as the
kinetoplastid protozoan parasites Trypanosoma brucei and Leishmania
major. Based on these findings, it is anticipated that the
hydroxamic acid and N-formyl hydroxylamine compounds with which
this invention is concerned have antiprotozoal activity, and are
useful in the treatment of malaria and other protozoal
diseases.
[0016] Certain N-formyl hydroxylamine derivatives have previously
been claimed in the patent publications listed below, although very
few examples of such compounds have been specifically made and
described:
TABLE-US-00001 EP-B-0236872 (Roche) WO 92/09563 (Glycomed) WO
92/04735 (Syntex) WO 95/19965 (Glycomed) WO 95/22966 (Sanofi
Winthrop) WO 95/33709 (Roche) WO 96/23791 (Syntex) WO 96/16027
(Syntex/Agouron) WO 97/03783 (British Biotech) WO 97/18207 (DuPont
Merck) WO 98/38179 (Glaxo-Wellcome) WO 98/47863 (Labs Jaques
Logeais) WO 99/06361 (Abbott Laboratories) WO 00/12082
(Glaxo-Wellcome) WO 00/12083 (Glaxo-Wellcome) WO 00/12466
(Glaxo-Wellcome) WO 00/12478 (Zeneca) WO 00/44712 (Abbott
Laboratories) WO 00/44739 (Abbott Laboratories) WO 00/59285 (DuPont
Pharmaceuticals)
[0017] The pharmaceutical utility ascribed to the N-formyl
hydroxylamine derivatives in those publications is the ability to
inhibit matrix metalloproteinases (MMPs) and in some cases release
of tumour necrosis factor (TNF), and hence the treatment of
diseases or conditions mediated by those enzymes, such as cancer
and rheumatoid arthritis.
[0018] In addition to these, U.S. Pat. No. 4,738,803 (Roques et
al.) also discloses N-formyl hydroxylamine derivatives, however,
these compounds are disclosed as enkephalinase inhibitors and are
proposed for use as antidepressants and hypotensive agents. Also,
WO 97/38705 (Bristol-Myers Squibb) and a recent publication (RobI
et al., Bioorg. Med. Chem. Lett., 10: 257-60, 2000) disclose
certain N-formyl hydroxylamine derivatives as enkephalinase and
angiotensin converting enzyme inhibitors.
[0019] Patent publications WO 99/41232 (British Biotech) and WO
00/43001 (British Biotech) respectively disclose the use of certain
N-formyl hydroxylamine derivatives as inhibitors of proliferation
of rapidly dividing cells and in the treatment of inflammation.
[0020] Very many hydroxamic acid derivatives are known. Many have
been disclosed as having matrix metalloproteinase (MMP) inhibitory
activity, and thus to be potentially useful for the treatment of
diseases mediated by MMPs, for example cancer, arthritides, and
contitions involving tissue remodeling such as wound healing, and
restenosis. WO 95/23790 (SmithKline Beecham) discloses MMP and
cytokine inhibiting hydroxamic acid derivatives of formula (A)
##STR00002##
wherein the variable R groups are as defined in the specification.
Similar compounds have been disclosed in WO 96/33176 (DuPont Merck)
and in Chen et. al., Bioorg. Med. Chem. Lett., 1996, 6, 1601-1606,
as inhibitors of MMPs and inhibitors of Tumour Necrosis Factor
production. Neither of these publications suggest that compounds
(A) have antibacterial or antiprotozoal activity.
[0021] Our copending International patent applications nos. WO
99/39704, WO 99/59568, WO 00/35440, WO 00/44373, WO 00/58294 and WO
00/61134 disclose that certain N-formyl hydroxylamine and
hydroxamic acid derivatives have antibacterial activity.
DETAILED DESCRIPTION OF THE INVENTION
[0022] According to the first aspect of the present invention there
is provided the use of a compound of formula (I) or a
pharmaceutically or veterinarily acceptable salt, hydrate or
solvate thereof in the preparation of a composition for treatment
of bacterial or protozoal infections in humans and non-human
mammals:
##STR00003##
wherein: Z represents a radical of formula --N(OH)CH(.dbd.O) or
formula --C(.dbd.O)NH(OH); R.sub.1 represents hydrogen, methyl or
trifluoromethyl, or, except when Z is a radical of formula
--N(OH)CH(.dbd.O), a hydroxy, halo or amino group; R.sub.2
represents a group R.sub.10--(X).sub.n-(ALK).sub.m-- wherein [0023]
R.sub.10 represents hydrogen, or a C.sub.1-C.sub.6 alkyl,
C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, cycloalkyl, aryl,
or heterocyclyl group, any of which may be unsubstituted or
substituted by (C.sub.1-C.sub.6)alkyl, (C.sub.1-C.sub.6)alkoxy,
hydroxy, mercapto, (C.sub.1-C.sub.6)alkylthio, amino, halo
(including fluoro, chloro, bromo and iodo), trifluoromethyl, cyano,
nitro, oxo, --COOH, --CONH.sub.2, --COOR.sup.A, NHCOR.sup.A,
--CONHR.sup.A, --NHR.sup.A, --NR.sup.AR.sup.B, or
--CONR.sup.AR.sup.B wherein R.sup.A and R.sup.B are independently a
(C.sub.1-C.sub.6)alkyl group and [0024] ALK represents a straight
or branched divalent C.sub.1-C.sub.6 alkylene, C.sub.2-C.sub.6
alkenylene, or C.sub.2-C.sub.6 alkynylene radical, and may be
interrupted by one or more non-adjacent --NH--, --O-- or --S--
linkages, [0025] X represents --NH--, --O-- or --S--, and [0026] m
and n are independently 0 or 1; R.sub.3 represents the side chain
of a natural or non-natural alpha amino acid; and R.sub.4
represents hydrogen, (C.sub.1-C.sub.6)alkyl or
phenyl(C.sub.1-C.sub.6)alkyl-; and [0027] (a) R.sub.5 and R.sub.6
independently represent: [0028] hydrogen, halogen, trifluoromethyl,
or [0029] (C.sub.1-C.sub.6)alkyl, (C.sub.2-C.sub.6)alkenyl,
(C.sub.2-C.sub.6)alkynyl, aryl, heterocyclyl,
aryl(C.sub.1-C.sub.6)alkyl-, or
heterocyclyl(C.sub.1-C.sub.6)alkyl-, any of which may be optionally
substituted by [0030] (C.sub.1-C.sub.6)alkyl, halogen,
trifluoromethyl, cyano, nitro, oxo, [0031] phenoxy or phenylthio-,
[0032] --OR.sup.A, --SR.sup.A, --NHR.sup.A, --NR.sup.AR.sup.B,
--NHCOR.sup.A--CONHR.sup.A, --CONR.sup.AR.sup.B, or --COOR.sup.A,
wherein [0033] R.sup.A and R.sup.B are independently hydrogen or
(C.sub.1-C.sub.4)alkyl, [0034] or in the case where R.sup.A and
R.sup.B are attached to a nitrogen atom then R.sup.A and R.sup.B
taken together with the nitrogen atom to which they are attached
form a monocyclic 5-7 membered ring; or [0035] (b) R.sub.5 and
R.sub.6 taken together with the carbon atoms to which they are
attached form a fused monocyclic or bicyclic carbocyclic or
heterocyclic ring which may be further substituted with any of the
substituent groups listed under (a).
[0036] In another aspect, the invention provides a method for the
treatment of bacterial or protozoal infections in humans and
non-human mammals, which comprises administering to a subject
suffering such infection an antibacterially or antiprotozoally
effective dose of a compound of formula (I) as defined above.
[0037] In a further aspect of the invention there is provided a
method for the treatment of bacterial contamination by applying an
antibacterially effective amount of a compound of formula (I) as
defined above to the site of contamination.
[0038] The compounds of formula (I) as defined above may be used as
component(s) of antibacterial cleaning or disinfecting
materials.
[0039] Compounds of formula (I) above wherein Z is a radical of
formula --N(OH)CH(.dbd.O), are believed to be novel. Accordingly,
in another aspect, the invention provides a compound of formula (I)
wherein Z is a radical of formula --N(OH)CH(.dbd.O), or a
pharmaceutically or veterinarily acceptable salt, hydrate or
solvate thereof. Furthermore, to the extent that compounds of
formula (I) above wherein Z is a radical of formula
--C(.dbd.O)NH(OH) do not form part of the state of the art, such
compounds and their pharmaceutically or veterinarily acceptable
salts, hydrates or solvates are also an aspect of the present
invention.
[0040] On the hypothesis that the compounds (I) act by inhibition
of intracellular PDF, the most potent antibacterial effect may be
achieved by using compounds which efficiently pass through the
bacterial cell wall. Thus, compounds which are highly active as
inhibitors of PDF in vitro and which penetrate bacterial cells are
preferred for use in accordance with the invention. It is to be
expected that the antibacterial potency of compounds which are
potent inhibitors of the PDF enzyme in vitro, but are poorly cell
penetrant, may be improved by their use in the form of a prodrug,
ie a structurally modified analogue which is converted to the
parent molecule of formula (I), for example by enzymic action,
after it has passed through the bacterial cell wall. The same is
true in the case of protozoa.
[0041] As used herein the term "(C.sub.1-C.sub.6)alkyl" means a
straight or branched chain alkyl moiety having from 1 to 6 carbon
atoms, including for example, methyl, ethyl, n-propyl, isopropyl,
n-butyl, isobutyl, sec-butyl, t-butyl, n-pentyl and n-hexyl.
[0042] As used herein the term "divalent (C.sub.1-C.sub.6)alkylene
radical" means a saturated hydrocarbon chain having from 1 to 6
carbon atoms and two unsatisfied valencies.
[0043] As used herein the term "(C.sub.2-C.sub.6)alkenyl" means a
straight or branched chain alkenyl moiety having from 2 to 6 carbon
atoms having at least one double bond of either E or Z
stereochemistry where applicable. The term includes, for example,
vinyl, allyl, 1- and 2-butenyl and 2-methyl-2-propenyl.
[0044] As used herein the term "divalent
(C.sub.2-C.sub.6)alkenylene radical" means a hydrocarbon chain
having from 2 to 6 carbon atoms, at least one double bond, and two
unsatisfied valencies.
[0045] As used herein the term "C.sub.2-C.sub.6 alkynyl" refers to
straight chain or branched chain hydrocarbon groups having from two
to six carbon atoms and having in addition one triple bond. This
term would include for example, ethynyl, 1-propynyl, 1- and
2-butynyl, 2-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl,
2-hexynyl, 3-hexynyl, 4-hexynyl and 5-hexynyl.
[0046] As used herein the term "divalent
(C.sub.2-C.sub.8)alkynylene radical" means a hydrocarbon chain
having from 2 to 6 carbon atoms, at least one triple bond, and two
unsatisfied valencies.
[0047] As used herein the term "cycloalkyl" means a saturated
alicyclic moiety having from 3-8 carbon atoms and includes, for
example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl,
cycloheptyl and cyclooctyl.
[0048] As used herein the term "cycloalkenyl" means an unsaturated
alicyclic moiety having from 3-8 carbon atoms and includes, for
example, cyclbpropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl,
cycloheptenyl and cyclooctenyl. In the case of cycloalkenyl rings
of from 5-8 carbon atoms, the ring may contain more than one double
bond.
[0049] As used herein the term "aryl" refers to a mono-, bi- or
tri-cyclic carbocyclic aromatic group, and to groups consisting of
two covalently linked monocyclic carbocyclic aromatic groups.
Illustrative of such groups are phenyl, biphenyl and napthyl.
[0050] As used herein the unqualified term "heterocyclyl" or
"heterocyclic" includes "heteroaryl" as defined below, and in
particular means a 5-8 membered aromatic or non-aromatic
heterocyclic ring containing one or more heteroatoms selected from
S, N and O, and optionally fused to a benzyl or second heterocyclic
ring, and the term includes, for example, pyrrolyl, furyl, thienyl,
piperidinyl, imidazolyl, oxazolyl, thiazolyl, thiadiazolyl,
thiazepinyl, pyrazolyl, pyridinyl, pyrrolidinyl, pyrimidinyl,
morpholinyl, piperazinyl, indolyl, and benzimidazolyl rings.
[0051] As used herein the term "heteroaryl" refers to a 5- or
6-membered aromatic ring containing one or more heteroatoms, and
optionally fused to a benzyl or pyridyl ring; and to groups
consisting of two covalently linked 5- or 6-membered aromatic rings
each containing one or more heteroatoms; and to groups consisting
of a monocyclic carbocyclic aromatic group covalently linked to a
5- or 6-membered aromatic rings containing one or more heteroatoms.
Illustrative of such groups are thienyl, furyl, pyrrolyl,
imidazolyl, benzimidazolyl, thiazolyl, pyrazolyl, isoxazolyl,
isothiazolyl, triazolyl, thiadiazolyl, oxadiazolyl, pyridinyl,
pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl,
4-([1,2,3]-thiadiazoly-4-yl)phenyl and 5-isoxazol-3-ylthienyl.
[0052] As used herein the unqualified term "carbocyclyl" or
"carbocyclic" refers to a 5-8 membered ring whose ring atoms are
all carbon.
[0053] Unless otherwise specified in the context in which it
occurs, the term "substituted" as applied to any moiety herein
means substituted with up to four substituents, each of which
independently may be (C.sub.1-C.sub.6)alkyl, phenyl, benzyl,
(C.sub.1-C.sub.6)alkoxy, phenoxy, hydroxy, mercapto,
(C.sub.1-C.sub.6)alkylthio, amino, halo (including fluoro, chloro,
bromo and iodo), trifluoromethyl, cyano, nitro, oxo, --COOH,
--CONH.sub.2, --COR.sup.A, --COOR.sup.A, --NHCOR.sup.A,
--CONHR.sup.A, --NHR.sup.A, --NR.sup.AR.sup.B, or
--CONR.sup.AR.sup.B wherein R.sup.A and R.sup.B are independently a
(C.sub.1-C.sub.6)alkyl group. In the case where "substituted" means
substituted by benzyl, the phenyl ring thereof may itself be
substituted with any of the foregoing, except phenyl or benzyl.
[0054] As used herein the terms "side chain of a natural
alpha-amino acid" and "side chain of a non-natural alpha-amino
acid" mean the group R.sup.x in respectively a natural and
non-natural amino acid of formula NH.sub.2--CH(R.sup.x)--COOH.
[0055] Examples of side chains of natural alpha amino acids include
those of alanine, arginine, asparagine, aspartic acid, cysteine,
cystine, glutamic acid, histidine, 5-hydroxylysine,
4-hydroxyproline, isoleucine, leucine, lysine, methionine,
phenylalanine, proline, serine, threonine, tryptophan, tyrosine,
valine, .alpha.-aminoadipic acid, .alpha.-amino-n-butyric acid,
3,4-dihydroxyphenylalanine, homoserine, .alpha.-methylserine,
ornithine, pipecolic acid, and thyroxine.
[0056] In natural alpha-amino acid side chains which contain
functional substituents, for example amino, carboxyl, hydroxy,
mercapto, guanidyl, imidazolyl, or indolyl groups as in arginine,
lysine, glutamic acid, aspartic acid, tryptophan, histidine,
serine, threonine, tyrosine, and cysteine, such functional
substituents may optionally be protected.
[0057] Likewise, in the side chains of non-natural alpha amino
acids which contain functional substituents, for example amino,
carboxyl, hydroxy, mercapto, guanidyl, imidazolyl, or indolyl
groups, such functional substituents may optionally be
protected.
[0058] The term "protected" when used in relation to a functional
substituent in a side chain of a natural or non-natural alpha-amino
acid means a derivative of such a substituent which is
substantially non-functional. The widely used handbook by T. W.
Greene and P. G. Wuts "Protective Groups in Organic Synthesis"
Second Edition, Wiley, New York, 1991 reviews the subject. For
example, carboxyl groups may be esterified (for example as a
C.sub.1-C.sub.6 alkyl ester), amino groups may be converted to
amides (for example as a NHCOC.sub.1-C.sub.6 alkyl amide) or
carbamates (for example as an NHC(.dbd.O)OC.sub.1-C.sub.6 alkyl or
NHC(.dbd.O)OCH.sub.2Ph carbamate), hydroxyl groups may be converted
to ethers (for example an OC.sub.1-C.sub.6 alkyl or a
O(C.sub.1-C.sub.6 alkyl)phenyl ether) or esters (for example a
OC(.dbd.O)C.sub.1-C.sub.6 alkyl ester) and thiol groups may be
converted to thioethers (for example a tert-butyl or benzyl
thioether) or thioesters (for example a SC(.dbd.O)C.sub.1-C.sub.6
alkyl thioester).
[0059] There are at least two actual or potential chiral centres in
the compounds according to the invention because of the presence of
asymmetric carbon atoms. The presence of several asymmetric carbon
atoms gives rise to a number of diastereoisomers with R or S
stereochemistry at each chiral centre. The invention includes all
such diastereoisomers and mixtures thereof. Currently, the
preferred stereoconfiguration of the carbon atom carrying the
R.sub.2 group is R; that of the carbon atom carrying the R.sub.1
group (when asymmetric) is R; and that of the carbon atom carrying
the R.sub.3 group (when asymmetric) is S
[0060] In the compounds of formula (I) as defined above:
[0061] When Z is a radical of formula --N(OH)CH(.dbd.O)R.sub.1 is
hydrogen, methyl or trifluoromethyl. When Z is a radical of formula
--C(.dbd.O)NH(OH)R.sub.1 is hydrogen, methyl, trifluoromethyl,
hydroxy, halo (e.g. chloro, bromo or especially fluoro) or amino.
Hydrogen is currently preferred in both cases.
[0062] R.sub.2 may be, for example: [0063] optionally substituted
C.sub.1-C.sub.8 alkyl, C.sub.3-C.sub.6 alkenyl, C.sub.3-C.sub.6
alkynyl or cycloalkyl; [0064] phenyl(C.sub.1-C.sub.6 alkyl)-,
phenyl(C.sub.3-C.sub.6 alkenyl)- or phenyl(C.sub.3-C.sub.6
alkynyl)-optionally substituted in the phenyl ring; [0065]
cycloalkyl(C.sub.1-C.sub.6 alkyl)-, cycloalkyl(C.sub.3-C.sub.6
alkenyl)- or cycloalkyl(C.sub.3-C.sub.6 alkynyl)- optionally
substituted in the cycloalkyl ring; [0066]
heterocyclyl(C.sub.1-C.sub.6 alkyl)-, heterocyclyl(C.sub.3-C.sub.6
alkenyl)- or [0067] heterocyclyl(C.sub.3-C.sub.6 alkynyl)-
optionally substituted in the heterocyclyl ring; or [0068]
CH.sub.3(CH.sub.2).sub.pO(CH.sub.2).sub.q-- or
CH.sub.3(CH.sub.2).sub.pS(CH.sub.2).sub.q--, wherein p is 0, 1, 2
or 3 and q is 1, 2 or 3.
[0069] Specific examples of R.sub.2 groups include [0070] methyl,
ethyl, n- and iso-propyl, n- and iso-butyl, n-pentyl, iso-pentyl
3-methyl-but-1-yl, n-hexyl, n-heptyl, n-acetyl, n-octyl,
methylsulfanylethyl, ethylsulfanylmethyl, 2-methoxyethyl,
2-ethoxyethyl, 2-ethoxymethyl, 3-hydroxypropyl, allyl,
3-phenylprop-3-en-1-yl, prop-2-yn-1-yl, 3-phenylprop-2-yn-1-yl,
3-(2-chlorophenyl)prop-2-yn-1-yl, but-2-yn-1-yl, cyclopentyl,
cyclohexyl, cyclopentylmethyl, cyclopentylethyl, cyclopentylpropyl,
cyclohexylmethyl, cyclohexylethyl, cyclohexylpropyl,
furan-2-ylmethyl, furan-3-methyl, tetrahydrofuran-2-ylmethyl,
tetrahydrofuran-2-ylmethyl, phenylpropyl, 4-chlorophenylpropyl,
4-methylphenylpropyl, 4-methoxyphenylpropyl, benzyl,
4-chlorobenzyl, 4-methylbenzyl, and 4-methoxybenzyl. [0071]
Presently preferred groups at R.sub.2 are n-propyl, n-butyl,
n-pentyl, and cyclopentylmethyl.
[0072] R.sub.3 may be, for example [0073] the characterising group
of a natural .alpha.-amino acid, for example benzyl, or
4-hydroxyphenylmethyl, in which any functional group may be
protected, any amino group may be acylated and any carboxyl group
present may be amidated; or [0074] a group -[Alk].sub.nR.sub.9
where Alk is a (C.sub.1-C.sub.6)alkylene or
(C.sub.2-C.sub.6)alkenylene group optionally interrupted by one or
more --O--, or --S-- atoms or --N(R.sub.12)-- groups [where
R.sub.12 is a hydrogen atom or a (C.sub.1-C.sub.6)alkyl group], n
is 0 or 1, and R.sub.9 is hydrogen or an optionally substituted
phenyl, aryl, heterocyclyl, cycloalkyl or cycloalkenyl group or
(only when n is 1) R.sub.9 may additionally be hydroxy, mercapto,
(C.sub.1-C.sub.6)alkylthio, amino, halo, trifluoromethyl, nitro,
--COOH, --CONH.sub.2, --COOR.sup.A, --NHCOR.sup.A, --CONHR.sup.A,
--NHR.sup.A, --NR.sup.AR.sup.B, or --CONR.sup.AR.sup.B wherein
R.sup.A and R.sup.B are independently a (C.sub.1-C.sub.6)alkyl
group; or [0075] a benzyl group substituted in the phenyl ring by a
group of formula --OCH.sub.2COR.sub.8 where R.sub.8 is hydroxyl,
amino, (C.sub.1-C.sub.6)alkoxy, phenyl(C.sub.1-C.sub.6)alkoxy,
(C.sub.1-C.sub.6)alkylamino, di((C.sub.1-C.sub.6)alkyl)amino,
phenyl(C.sub.1-C.sub.6)alkylamino; or [0076] a
heterocyclic(C.sub.1-C.sub.6)alkyl group, either being
unsubstituted or mono- or di-substituted in the heterocyclic ring
with halo, nitro, carboxy, (C.sub.1-C.sub.6)alkoxy, cyano,
(C.sub.1-C.sub.6)alkanoyl, trifluoromethyl (C.sub.1-C.sub.6)alkyl,
hydroxy, formyl, amino, (C.sub.1-C.sub.6)alkylamino,
di-(C.sub.1-C.sub.6)alkylamino, mercapto,
(C.sub.1-C.sub.6)alkylthio, hydroxy(C.sub.1-C.sub.6)alkyl,
mercapto(C.sub.1-C.sub.6)alkyl or
(C.sub.1-C.sub.6)alkylphenylmethyl; or [0077] a group
--CR.sub.aR.sub.bR.sub.c in which: [0078] each of R.sub.a, R.sub.b
and R.sub.c is independently hydrogen, (C.sub.1-C.sub.6)alkyl,
(C.sub.2-C.sub.6)alkenyl, (C.sub.2-C.sub.6)alkynyl,
phenyl(C.sub.1-C.sub.6)alkyl, (C.sub.3-C.sub.8)cycloalkyl; or
[0079] R.sub.c is hydrogen and R.sub.a and R.sub.b are
independently phenyl or heteroaryl such as pyridyl; or [0080]
R.sub.c is hydrogen, (C.sub.1-C.sub.6)alkyl,
(C.sub.2-C.sub.6)alkenyl, (C.sub.2-C.sub.6)alkynyl,
phenyl(C.sub.1-C.sub.6)alkyl, or (C.sub.3-C.sub.8)cycloalkyl, and
R.sub.a and R.sub.b together with the carbon atom to which they are
attached form a 3 to 8 membered cycloalkyl or a 5- to 6-membered
heterocyclic ring; or [0081] R.sub.a, R.sub.b and R.sub.c together
with the carbon atom to which they are attached form a tricyclic
ring (for example adamantyl); or [0082] R.sub.a and R.sub.b are
each independently (C.sub.1-C.sub.6)alkyl,
(C.sub.2-C.sub.6)alkenyl, (C.sub.2-C.sub.6)alkynyl,
phenyl(C.sub.1-C.sub.6)alkyl, or a group as defined for R.sub.c
below other than hydrogen, or R.sub.a and R.sub.b together with the
carbon atom to which they are attached form a cycloalkyl or
heterocyclic ring, and R.sub.c is hydrogen, --OH, --SH, halogen,
--CN, --CO.sub.2H, (C.sub.1-C.sub.4)perfluoroalkyl, --CH.sub.2OH,
--CO.sub.2(C.sub.1-C.sub.6)alkyl, --O(C.sub.1-C.sub.6)alkyl,
--O(C.sub.2-C.sub.6)alkenyl, --S(C.sub.1-C.sub.6)alkyl,
--SO(C.sub.1-C.sub.6)alkyl, --SO.sub.2(C.sub.1-C.sub.6) alkyl,
--S(C.sub.2-C.sub.6)alkenyl, --SO(C.sub.2-C.sub.6)alkenyl,
--SO.sub.2(C.sub.2-C.sub.6)alkenyl or a group -Q-W wherein Q
represents a bond or --O--, --S--, --SO-- or --SO.sub.2-- and W
represents a phenyl, phenylalkyl, (C.sub.3-C.sub.8)cycloalkyl,
(C.sub.3-C.sub.8)cycloalkylalkyl, (C.sub.4-C.sub.8)cycloalkenyl,
(C.sub.4-C.sub.8)cycloalkenylalkyl, heteroaryl or heteroarylalkyl
group, which group W may optionally be substituted by one or more
substituents independently selected from, hydroxyl, halogen, --CN,
--CO.sub.2H, --CO.sub.2(C.sub.1-C.sub.6)alkyl, --CONH.sub.2,
--CONH(C.sub.1-C.sub.6)alkyl, --CONH(C.sub.1-C.sub.6alkyl).sub.2,
--CHO, --CH.sub.2OH, (C.sub.1-C.sub.4)perfluoroalkyl,
--O(C.sub.1-C.sub.6)alkyl, --S(C.sub.1-C.sub.6)alkyl,
--SO(C.sub.1-C.sub.6)alkyl, --SO.sub.2(C.sub.1-C.sub.6)alkyl,
--NO.sub.2, --NH.sub.2, --NH(C.sub.1-C.sub.6)alkyl,
--N((C.sub.1-C.sub.8)alkyl).sub.2, --NHCO(C.sub.1-C.sub.6)alkyl,
(C.sub.1-C.sub.6)alkyl, (C.sub.2-C.sub.6)alkenyl,
(C.sub.2-C.sub.6)alkynyl, (C.sub.3-C.sub.8)cycloalkyl,
(C.sub.4-C.sub.8)cycloalkenyl, phenyl or benzyl. [0083] Examples of
particular R.sub.3 groups include methyl, ethyl, benzyl,
4-chlorobenzyl, 4-hydroxybenzyl, phenyl, cyclohexyl,
cyclohexylmethyl, pyridin-3-ylmethyl, tert-butoxymethyl,
naphthylmethyl, iso-butyl, sec-butyl, tert-butyl,
1-benzylthio-1-methylethyl, 1-methylthio-1-methylethyl,
1-mercapto-1-methylethyl, 1-methoxy-1-methylethyl,
1-hydroxy-1-methylethyl, 1-fluoro-1-methylethyl, hydroxymethyl,
2-hydroxethyl, 2-carboxyethyl, 2-methylcarbamoylethyl,
2-carbamoylethyl, and 4-aminobutyl. Presently preferred R.sub.3
groups include tert-butyl.
[0084] R.sub.4 may be, for example, hydrogen, methyl or ethyl.
[0085] R.sub.5 and R.sub.6 may independently be, for example,
hydrogen, methyl, trifluoromethyl, phenyl, bromo, chloro, fluoro,
methoxy, hydroxymethyl, dimethylaminomethyl-, ethoxymethyl-,
4-methyl-piperazine-1-carbonyl-, 4-methyl-piperazin-1-ylmethyl-,
morpholin-4-ylmethyl-, methoxycarbonyl, thiazol-2-yl-,
phenoxymethyl-, pyrrolidin-1-ylmethyl-, piperidin-1-ylmethyl-,
--C(O)NH.sub.2, (CH.sub.2).sub.2CO.sub.2CH.sub.3,
--CH(OH)CH(CH.sub.3).sub.2, --CH(OH)CH.sub.3, --CH(OH)Ph, or
R.sub.5 and R.sub.6 taken together with the carbon atoms to which
they are attached may form a fused benzo, naphtho or pyrido, for
example a [4,5-c]pyridin-2-yl, ring, which may be substituted as
specified, for example a fused benzo ring substituted by methyl,
cyano, hydroxy, chloro or fluoro in the 4- or 5-position.
[0086] Specific examples of compounds within or for use within the
scope of the invention include the following N-formyl hydroxylamine
derivatives, and their corresponding hydroxamic acid analogues:
[0087]
2R-Cyclopentylmethyl-N-[1S-(5-fluoro-1H-benzoimidazol-2-yl)-2,2-dimethyl--
propyl]-3-(formyl-hydroxy-amino)-propionamide; [0088]
N-[1-(5-Chloro-1H-benzoimidazol-2-yl)-2,2-dimethyl-propyl]-2-cyclopentylm-
ethyl-3-(formyl-hydroxy-amino)-propionamide; [0089]
N-[1-(1H-Benzoimidazol-2-yl)-2,2-dimethyl-propyl]-2-cyclopentylmethyl-3-(-
formyl-hydroxy-amino)-propionamide; [0090]
2-[(Formyl-hydroxy-amino)-methyl]-hexanoic acid
[1-(1H-benzoimidazol-2-yl)-2,2-dimethyl-propyl]-amide; [0091]
3-Cyclopentyl-N-[1S-(6-dimethylaminomethyl-1H-benzoimidazol-2-yl)-2,2-dim-
ethyl-propyl]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide;
[0092]
3-Cyclopentyl-N-[1S-(6-dimethylaminomethyl-1-methyl-1H-benzoimidazol-2-yl-
)-2,2-dimethyl-propyl]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide;
[0093]
N-(1S-{6-[(Acetyl-methyl-amino)-methyl]-1H-benzoimidazol-2-yl}2,2--
dimethyl-propyl)-3-cyclopentyl-2R-[(formyl-hydroxy-amino)-methyl]-propiona-
mide; [0094]
3-Cyclopentyl-2R-[(formyl-hydroxy-amino)-methyl]-N-[1S-(6-hydroxymethyl-1-
H-benzoimidazol-2-yl)-2,2-dimethyl-propyl]-propionamide; [0095]
3-Cyclopentyl-N-[1S-(5-dimethylaminomethyl-1H-imidazol-2-yl)-2,2-dimethyl-
-propyl]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide; [0096]
3-Cyclopentyl-N-[1S-(6-ethoxymethyl-1H-benzoimidazol-2-yl)-2,2-dimethyl-p-
ropyl]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide; [0097]
3-Cyclopentyl-N-[1S-(5-ethoxymethyl-1H-imidazol-2-yl)-2,2-dimethyl-propyl-
]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide; [0098]
N-[1S-(5-{[(Benzo[1,3]dioxol-5-ylmethyl)-amino]-methyl}-1H-imidazol-2-yl)-
-2,2-dimethyl-propyl]-3-cyclopentyl-2R-[(formyl-hydroxy-amino)-methyl]-pro-
pionamide; [0099]
3-Cyclopentyl-2R-[(formyl-hydroxy-amino)-methyl]-N-[1S-(1H-imidazo[4,5-c]-
pyridin-2-yl)-2,2-dimethyl-propyl]-propionamide; [0100]
3-Cyclopentyl-N-[1S-(1-ethyl-1H-imidazo[4,5-c]pyridin-2-yl)-2,2-dimethyl--
propyl]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide; [0101]
3-Cyclopentyl-N-{2,2-dimethyl-1S-[5-(4-methyl-piperazine-1-carbonyl)-1H-i-
midazol-2-yl]-propyl}-2R-[(formyl-hydroxy-amino)-methyl]-propionamide;
[0102]
3-Cyclopentyl-N-{2,2-dimethyl-1S-[5-(4-methyl-piperazin-1-ylmethyl-
)-1H-imidazol-2-yl]-propyl}-2R-[(formyl-hydroxy-amino)-methyl]-propionamid-
e; [0103]
3-Cyclopentyl-N-[2,2-dimethyl-1S-(5-morpholin-4-ylmethyl-1H-imid-
azol-2-yl)-propyl]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide;
[0104]
3-Cyclopentyl-2R-[(formyl-hydroxy-amino)-methyl]-N-[1S-(1H-imidazol-2-yl)-
-2,2-dimethyl-propyl]-propionamide; [0105]
2-(1S-{3-Cyclopentyl-2R-[(formyl-hydroxy-amino)-methyl]-propionylamino}-2-
,2-dimethyl-propyl)-3H-imidazole-4-carboxylic acid methyl ester;
[0106]
3-Cyclopentyl-N-[2,2-dimethyl-1S-(5-thiazol-2-yl-1H-imidazol-2-yl)-propyl-
]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide; [0107]
3-Cyclopentyl-N-[2,2-dimethyl-1S-(5-phenoxymethyl-1H-imidazol-2-yl)-propy-
l]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide; [0108]
3-Cyclopentyl-N-[2,2-dimethyl-1S-(5-pyrrolidin-1-ylmethyl-1H-imidazol-2-y-
l)-propyl]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide; and
[0109]
3-Cyclopentyl-N-[2,2-dimethyl-1S-(5-piperidin-1-ylmethyl-1H-imidazol-2-yl-
)-propyl]-2R-[(formyl-hydroxy-amino)-methyl]-propionamide.
[0110] Compounds of the invention wherein Z is a radical of formula
--N(OH)CH(.dbd.O) may be prepared by deprotection of a compound of
formula (II)
##STR00004##
wherein P represents a hydroxy protecting group, and R.sub.1,
R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are as defined in
relation to formula (II). Compounds of formula (II) may be prepared
by coupling a carboxylic acid of formula (III),
##STR00005##
with an amine of formula (IV) using standard peptide coupling
methods. Carboxylic acids of formula (III) may be prepared by
analogy with the methods described in WO 99/39704. Amines of
formula (IV) may be prepared according to any of a variety of
methods described in the literature (Chen et al., Bioorg. Med.
Chem. Lett., 1996, 6, 1601-1606; Gordon et al., Tetrahedron Lett.
34, 1901-1904, 1993; Gordon et al., Bioorg. Med. Chem. Lett., 1993,
3, 915-920; Abdel-Meguid et al., Biochemistry 33:11671-7, 1994) and
in (WO 93/02057, 95/23790 and WO 96/33176.
[0111] Hydroxamate compounds of formula (I) for use in accordance
with the invention may be prepared by reacting a compound of
formula (V) or a carboxyl-activated derivative thereof
##STR00006##
with hydroxylamine or an N- and/or O-protected hydroxylamine, and
thereafter removing any O- or N-protecting groups.
Carboxyl-activated derivatives of compound (V) include
1-hydroxybenzotriazole ester and pentafluorophenyl ester. A
compound of formula (V) may be prepared by standard peptide
coupling methods from a carboxylic acid of formula (VI), wherein P
is as defined in relation to formula (II), and an amine of formula
(IV), followed by removal of P.
##STR00007##
[0112] Compounds of formula (VI) are well known starting materials
in the synthesis of matrix metalloproteinase inhibitors.
[0113] Antibacterial or antiprotozoal compositions with which the
invention is concerned may be prepared for administration by any
route consistent with the pharmacokinetic properties of the active
ingredient(s).
[0114] Orally administrable compositions may be in the form of
tablets, capsules, powders, granules, lozenges, liquid or gel
preparations, such as oral, topical, or sterile parenteral
solutions or suspensions. Tablets and capsules for oral
administration may be in unit dose presentation form, and may
contain conventional excipients such as binding agents, for example
syrup, acacia, gelatin, sorbitol, tragacanth, or
polyvinyl-pyrrolidone; fillers for example lactose, sugar,
maize-starch, calcium phosphate, sorbitol or glycine; tabletting
lubricant, for example magnesium stearate, talc, polyethylene
glycol or silica; disintegrants for example potato starch, or
acceptable wetting agents such as sodium lauryl sulphate. The
tablets may be coated according to methods well known in normal
pharmaceutical practice. Oral liquid preparations may be in the
form of, for example, aqueous or oily suspensions, solutions,
emulsions, syrups or elixirs, or may be presented as a dry product
for reconstitution with water or other suitable vehicle before use.
Such liquid preparations may contain conventional additives such as
suspending agents, for example sorbitol, syrup, methyl cellulose,
glucose syrup, gelatin hydrogenated edible fats; emulsifying
agents, for example lecithin, sorbitan monooleate, or acacia;
non-aqueous vehicles (which may include edible oils), for example
almond oil, fractionated coconut oil, oily esters such as
glycerine, propylene glycol, or ethyl alcohol; preservatives, for
example methyl or propyl p-hydroxybenzoate or sorbic acid, and if
desired conventional flavouring or colouring agents.
[0115] For topical application to the skin, the active
ingredient(s) may be made up into a cream, lotion or ointment.
Cream or ointment formulations which may be used for the drug are
conventional formulations well known in the art, for example as
described in standard textbooks of pharmaceutics such as the
British Pharmacopoeia.
[0116] The active ingredient(s) may also be administered
parenterally in a sterile medium. Depending on the vehicle and
concentration used, the drug can either be suspended or dissolved
in the vehicle. Advantageously, adjuvants such as a local
anaesthetic, preservative and buffering agents can be dissolved in
the vehicle. Intra-venous infusion is another route of
administration for the compounds used in accordance with the
invention.
[0117] Safe and effective dosages for different classes of patient
and for different disease states will be determined by clinical
trial as is required in the art. It will be understood that the
specific dose level for any particular patient will depend upon a
variety of factors including the activity of the specific compound
employed, the age, body weight, general health, sex, diet, time of
administration, route of administration, rate of excretion, drug
combination and the severity of the particular disease undergoing
therapy.
[0118] The following examples illustrate embodiments of the
invention. .sup.1H and spectra were recorded using a Bruker DPX 250
spectrometer at 250.1 MHz. Mass spectra were obtained using a
Perkin Elmer Sciex API 165 spectrometer using both positive and
negative ionisation modes. Analytical HPLC was performed on a
Beckman System Gold, using Waters Nova Pak C18 column (150 mm, 3.9
mm) with 20 to 90% solvent B gradient (1 ml/min) as the mobile
phase. [Solvent A: 0.05% TFA in 10% water 90% methanol; Solvent B:
0.05% TFA in 10% methanol 90%], detection wavelength at 214 nm.
Preparative HPLC was performed on a Gilson autoprep instrument
using a C18 Waters delta prep-pak cartridge (15 .mu.m, 300 A, 25
mm, 10 mm) with 20 to 90% solvent B gradient (6 ml/min) as the
mobile phase. [Solvent A water; Solvent B: methanol], UV detection
was at 214 nm.
[0119] The following abbreviations have been used throughout:
EDC N-Ethyl-N'-(3-dimethylaminopropyl)carbodiimide hydrochloride
HPLC High performance liquid chromatography LRMS Low resolution
mass spectrometry NMR Nuclear magnetic resonance
RT Retention Time
EXAMPLE 1
2R-Cyclopentylmethyl-N-[1S-(5-fluoro-1H-benzoimidazol-2-yl)-2,2-dimethyl-p-
ropyl]-3-(formyl-hydroxy-amino)-propionamide
##STR00008##
[0121] The title compound was prepared as outlined in Scheme 1 and
is described in detail below.
##STR00009##
Step A
Compound 1:
[1S-(2-Amino-5-fluoro-phenylcarbamoyl)-2,2-dimethyl-propyl]-carbamic
acid benzyl ester
Compound 2:
[1S-(2-Amino-4-fluoro-phenylcarbamoyl)-2,2-dimethyl-propyl]-carbamic
acid benzyl ester
[0122] To a solution of Z-tert-leucine (4.04 g, 1.54 mmol) in
dichloromethane (15 ml), was added the 1,2-diamine (2.57 g, 1.68
mmol) followed by EDC (3.21 g, 1.68 mmol). The resulting reaction
mixture was stirred at room temperature for 12 hrs. The reaction
mixture was then diluted with dichloromethane and washed with water
(30 ml), 1M aq. Na.sub.2CO.sub.3 (30 ml), 1M HCl (20 ml) and brine.
The combined organic layers were dried over anhydrous MgSO.sub.4,
filtered and the solvent was removed in vacuo to yield a pale
yellow foam which was purified by flash chromatography
(hexane:ethyl acetate, 3:1) to give a mixture of regioisomeric
compounds, 1 and 2. A further purification by flash chromatography
afforded compound 1 as a pure solid (2.44 g, 43% yield).
.sup.1H-NMR; .delta. (CDCl.sub.3, mixture of 1 and 2), 7.71 (1H, br
s), 7.38-7.27 (5H, m), 7.04-6.98 (1H, m), 6.44-6.36 (2H, m), 5.63
(1H, br d), 5.13-4.99 (2H, AB system), 4.16-4.08 (1H, m), 3.94 (2H,
br s), 1.09 (9H, s).
[0123] (N.B. Both 1 and 2 give the same compound after
cyclisation.)
Step B:
[1S-(5-Fluoro-1H-benzoimidazol-2-yl)-2,2-dimethyl-propyl]-carbamic
acid benzyl ester
[0124] A solution of the mixture of 1 and 2 (2.24 g, 6.45 mmol) in
glacial acetic acid (25 ml) was heated to 65.degree. C. for 12 hrs.
Acetic acid was removed under reduced pressure. The resulting salt
was partitioned between dichloromethane and 1M aq.
Na.sub.2CO.sub.3. The organic layer was washed with brine, dried
over anhydrous MgSO.sub.4, filtered and the solvent was removed
under reduced pressure. The resulting crude reaction mixture was
purified by flash chromatography (hexane/ethyl acetate: 3/1) to
give the title compound (1.92 g, 84% yield). LRMS: +ve ion 356
[M+1], -ve ion 354 [M-1]; HPLC data: RT 5.13 min.
Step C:
1S-(6-Fluoro-1H-benzoimidazol-2-yl)-2,2-dimethyl-propylamine
[0125] To a cold (5.degree. C.) solution of
[1S-(5-fluoro-1H-benzoimidazol-2-yl)-2,2-dimethyl-propyl]-carbamic
acid benzyl ester (400 mg, 1.13 mmol) in acetic acid (10 ml) was
added 48% HBr in H.sub.2O (12 ml). The resulting reaction mixture
was stirred for 4 hrs at room temperature. Solvent was then removed
under reduced pressure. The crude salt was dissolved in ethyl
acetate and washed with 1M aq. Na.sub.2CO.sub.3 and brine. The
organic layer was dried over anhydrous MgSO.sub.4, filtered and the
solvent removed in vacuo to provide the title compound (230 mg,
92%). .sup.1H-NMR; .delta. (CDCl.sub.3), 7.51-7.44 (1H, dd, J=8.73,
4.73 Hz), 7.28-7.21 (1H, m), 7.02-6.93 (1H, m), 4.05 (1H, s), 1.04
(9H, s).
Step D:
4-Benzyloxy-2R-cyclopentylmethyl-N-[1S-(6-fluoro-1H-benzoimidazol--
2-yl)-2,2-dimethyl-propyl]-4-formylamino-butyramide
[0126] To a solution of the
4-benzyloxy-2R-cyclopentylmethyl-4-formylamino-butyric acid
pentafluorophenyl ester (426 mg, 9.05 mmol) in dichloromethane (6
ml) was added
1S-(6-fluoro-1H-benzoimidazol-2-yl)-2,2-dimethyl-propylamine (from
Step C) (220 mg, 1.00 mmol), followed bytriethylamine (189 .mu.l,
1.36 mmol). The resulting reaction mixture was stirred for 12 hrs
at room temperature. The reaction mixture was diluted with
dichloromethane and washed with water (20 ml), 1M aq.
Na.sub.2CO.sub.3 and brine. The organic layer was dried over
anhydrous MgSO.sub.4, filtered and the solvent was removed in
vacuo. The residual yellow solid was purified by flash
chromatography (hexanes/ethyl acetate from 1:2 to 1:5) to provide
the title compound (270 mg, 59%).
Step E:
2R-Cyclopentylmethyl-N-[1-(5-fluoro-1H-benzoimidazol-2-yl)-2,2-dim-
ethyl-propyl]-3-(formyl-hydroxy-amino)-propionamide
[0127] To a solution of
4-benzyloxy-2R-cyclopentylmethyl-N-[1S-(6-fluoro-1H-benzoimidazol-2-yl)-2-
,2-dimethyl-propyl]-4-formylamino-butyramide (113 mg, 2.22 mmol) in
ethanol (100 ml), under a blanket of argon, was added 10% palladium
on charcoal (10 mg). Hydrogen was bubbled through the suspension
for 15 min and the reaction was stirred under an atmosphere of
hydrogen for 15 min. The palladium catalyst was filtered off and
the solvent was removed in vacuo to yield the title compound as a
white foam (73 mg, 78%). .sup.1H-NMR; .delta. (CDCl.sub.3), 8.41
(0.4H, br s), 7.94 (0.6H, br s), 7.60-7.09 (2H, m), 6.91 (1H, m),
6.43 (1H, m), 5.31 (0.5H, d), 5.16 (0.5H, d), 4.08 (0.5H, m), 3.93
(0.5H, m), 3.75 (0.5H, m), 3.58 (0.5H, m), 3.25 (0.5H, m), 3.02
(0.5H, m), 1.80-0.80 (11H, m), 1.02 (9H, s). HPLC data: RT 4.93
min.
[0128] The compounds of Examples 2-3 and 5-8 were prepared by
analogy with Example 1 starting from the appropriate 1,2
diaminobenzene. The compound of Example 4 was prepared in a similar
manner using 2R-[(benzoyloxy-formylamino)-methyl]-hexanoic acid in
place of 4-benzyloxy-2R-cyclopentylmethyl-4-formylaminobutyric acid
pentafluorophenyl ester.
EXAMPLE 2
N-[1-(5-Chloro-1H-benzoimidazol-2-yl)-2,2-dimethyl-propyl]-2-cyclopentylme-
thyl-3-(formyl-hydroxy-amino)-propionamide
##STR00010##
[0130] .sup.1H-NMR; .delta. (CDCl.sub.3), 8.44 (0.4H, s), 7.95
(0.6H, s), 7.71-7.48 (1H, m), 7.30-7.02 (2H, m), 5.30 (0.5H, d, J=9
Hz), 5.14 (0.5H, br s), 4.01-3.89 (1H, m), 3.80 (0.5H, d, J=12 Hz),
3.60 (0.5H, d, J=12 Hz), 3.23 (0.4H, br s), 3.01 (0.6H, br s) and
1.85-0.80 (20H, m). HPLC data: RT 4.84 min. LRMS: +ve ion 435
[M+1], -ve ion 433 [M-1].
EXAMPLE 3
N-[1-(1H-Benzoimidazol-2-yl)-2,2-dimethyl-propyl]-2-cyclopentylmethyl-3-(f-
ormyl-hydroxy-amino)-propionamide
##STR00011##
[0132] .sup.1H-NMR; .delta. (CDCl.sub.3), 8.43 (0.5H, br s), 7.95
(0.5H, br s), 7.68 (1H, br s), 7.48-7.10 (4H, m), 5.39 (0.5H, d,
J=9.6 Hz), 5.26 (0.5H, d, J=8 Hz), 4.11 (0.5H, m), 3.98-3.94 (0.5H,
dd, J=10.8, 13.3 Hz), 3.72 (0.5H, m), 3.59 (0.5H, d, J=11.8 Hz),
3.26 (0.5H, br s), 3.04 (0.5H, br s) and 1.73-0.81 (20H, m). HPLC
data: RT 4.42 min.
EXAMPLE 4
2-[(Formyl-hydroxy-amino)-methyl]-hexanoic acid
[1-(1H-benzoimidazol-2-yl)-2,2-dimethyl-propyl]-amide
##STR00012##
[0134] .sup.1H-NMR; .delta. (CD.sub.3OD), 8.28 (0.3H, s), 7.85
(0.7H, s), 7.54 (2H, br s), 7.22 (2H, dd, J=6.1, 3.1 Hz), 5.09
(0.7H, s), 5.07 (0.3H, s), 3.84-3.78 (0.3H, m), 3.79 (0.7H, dd,
J=14.2, 9.5 Hz), 3.63 (0.3H, dd, J=14.0, 5.5 Hz), 3.44 (0.7H, dd,
J=14.2, 4.6 Hz), 3.17-2.97 (0.7H, m), 2.88-2.82 (0.3H, m),
1.58-1.35 (2H, m), 1.23-1.02 (4H, m), 1.04 (2.7H, s), 1.02 (6.3H,
s), 0.65 (0.9H, t, J=6.8 Hz) and 0.63 (2.1H, t, J=7.1 Hz).
EXAMPLE 5
2R-Cyclopentylmethyl-N-[2,2-dimethyl-1S-(1H-naphtho[2,3-d]imidazol-2-yl)-p-
ropyl]-3-(formyl-hydroxy-amino)-propionamide
##STR00013##
[0136] .sup.1H-NMR; .delta. (DMSO), 10.06 (0.4H, s), 9.53 (0.6H,
s), 8.30 (1.3H, m), 8.12 (1H, s), 7.97 (2H, d, J=9.3 Hz), 7.94 (1H,
s), 7.81 (0.7H, s), 7.35 (2H, br s), 5.10 (1H, m), 3.63 (1H, m),
3.47 (0.6H, m), 3.32 (0.4H, m), 2.94 (1H, m), 1.67 (1H, m), 1.36
(2H, m), 1.08 (2H, m) 0.99 (9H, s) and 0.87 (2H, m). .sup.13C-NMR;
.delta. (DMSO), 173.4, 158.7, 158.5, 144.1, 134.7, 130.2, 129.7,
128.3, 127.7, 123.9, 123.2, 115.1, 106.8, 56.1, 52.5, 49.1, 43.2,
43.0, 37.9, 37.7, 36.1, 35.5, 32.6, 32.4, 32.3, 27.0 and 24.7.
LCMS: +ve ion 451 [M+H], for major peak. HPLC: RT=3.54 min.
EXAMPLE 6
2R-Cyclopentylmethyl-N-[2,2-dimethyl-1S-(5-methyl-1H-benzoimidazol-2-yl)-p-
ropyl]-3-(formyl-hydroxy-amino)-propionamide
##STR00014##
[0138] .sup.1H-NMR; .delta. (CH.sub.3OD), 8.29 (0.3H, s), 7.85
(0.7H, s), 7.41 (1H, d, J=8.1 Hz), 7.32 (1H, s), 7.05 (1H, d, J=8.2
Hz), 5.08 (1H, m), 3.80 (1H, m), 3.62 (0.3H, m), 3.44 (0.7H, m),
3.05 (0.7H, m), 2.91 (0.3H, m), 2.44 (3H, s), 1.41 (9H, m), 1.04
(3H, s), 1.01 (6H, s), 0.93 (2H, m). .sup.13C-NMR; .delta.
(CH.sub.3OD), 176.5, 176.2, 164.4, 159.7, 154.5, 154.3, 133.9,
125.5, 73.0, 70.3, 65.1, 58.4, 58.3, 54.3, 50.7, 45.9, 45.8, 39.6,
37.9, 37.8, 37.6, 37.1, 36.8, 34.2, 34.1, 34.0, 27.5, 26.3 and
22.1. LRMS: +ve ion 415 [M+H], 437 [M+Na]. HPLC: RT=5.16 min
EXAMPLE 7
2R-Cyclopentylmethyl-3-(formyl-hydroxy-amino)-N-[1S-(4-hydroxy-1H-benzoimi-
dazol-2-yl)-2,2-dimethyl-propyl]-propionamide
##STR00015##
[0140] .sup.1H-NMR; .delta. (CH.sub.3OD), 8.28 (0.4H, s), 7.84
(0.6H, s), 7.01 (2H, m), 6.61 (1H, m), 5.09 (1H, m), 3.80 (1H, m),
3.62 (0.3H, m), 3.45 (0.7H, m), 2.87 (0.3H, m), 1.73 (1H, m), 1.38
(8H, m), 1.03 (3H, s), 1.01 (6H, s), 0.93 (2H, m). .sup.13C-NMR; 6
(CH.sub.3OD), 176.4, 176.2, 164.3, 159.6, 153.2, 124.7, 108.4,
58.1, 54.3, 50.7, 46.0, 45.9, 39.7, 39.6, 37.9, 36.9, 34.1, 34.0,
27.5, 26.2 and 26.1. LRMS: +ve ion 417 [M+H], 439 [M+Na]. HPLC:
RT=4.62 min.
EXAMPLE 8
N-[1S-(5-Cyano-1H-benzoimidazol-2-yl)-2,2-dimethyl-propyl]-2R-cyclopentylm-
ethyl-3-(formyl-hydroxy-amino)-propionamide
##STR00016##
[0142] .sup.1H-NMR; .delta. (CH.sub.3OD), 8.29 (0.4H, s), 7.96 (1H,
s), 7.86 (1H, d, J=8.3 Hz), 7.54 (1H, d, J=8.3 Hz), 5.11 (1H, m),
3.80 (1H, m), 3.61 (0.4H, m), 3.46 (0.6H, m), 3.10 (0.6H, m), 2.90
(0.4H, m), 1.41 (11H, m), 1.06 (3H, s) and 1.04 (6H, s).
.sup.13C-NMR; .delta. (CH.sub.3OD), 176.8, 176.5, 164.4, 159.7,
158.7, 158.5, 127.4, 121.1, 106.7, 58.7, 58.4, 54.2, 50.7, 48.0,
45.6, 39.6, 37.9, 37.8, 36.6, 35.2, 34.5, 34.1, 34.0, 27.7, 27.4,
26.5, 26.2 and 18.8. LRMS: +ve ion 426 [M+H], -ve ion 424 [M-H].
HPLC: RT=5.29 min.
[0143] Examples 9 & 10 were prepared by analogy with Example 1
using glycine in place of t-leucine.
EXAMPLE 9
N-(1H-Benzoimidazol-2-ylmethyl)-2R-cyclopentylmethyl-3-(formyl-hydroxy-ami-
no)-propionamide
##STR00017##
[0145] .sup.1H-NMR; .delta. (CH.sub.3OD), 8.32 (0.5H, s), 7.89
(0.5H, s), 7.54 (2H, m), 7.22 (2H, m), 4.85 (1H, m), 4.42 (1H, m),
3.96 (0.1H, dd, J=13.9 4.3 Hz), 3.83 (0.4H, dd, J=13.8, 4.8 Hz),
3.69 (1H, m), 3.56 (0.5H, dd, J=14.1, 4.8 Hz), 2.93 (0.5H, m), 2.80
(0.5H, m), 1.61 (9H, m) and 1.11 (2H, m). .sup.13C-NMR; .delta.
(CH.sub.3OD), 177.5, 177.0, 164.6, 160.4, 153.7, 153.3, 124.1,
116.3, 116.1, 54.2, 53.8, 51.8, 46.5, 46.2, 46.0, 39.7, 39.6, 38.6,
38.3, 38.2, 37.7, 37.5, 34.4, 33.9, 33.8, 26.4 and 20.9. LRMS: +ve
ion 345 [M+H], 367 [M+Na]. HPLC: RT=4.72 min.
EXAMPLE 10
2R-Cyclopentylmethyl-3-(formyl-hydroxy-amino)-N-(5-methyl-1H-benzoimidazol-
-2-ylmethyl)-propionamide
##STR00018##
[0147] .sup.1H-NMR; .delta. (CH.sub.3OD), 8.31 (0.5H, s), 7.89
(0.5H, s), 7.36 (2H, m), 7.04 (1H, d, J=7.9 Hz), 4.80 (1H, m), 4.39
(1H, m), 3.69 (2H, m), 2.92 (0.5H, m), 2.80 (0.5H, m), 2.43 (3H,
s), 1.60 (9H, m) and 1.13 (2H, m). .sup.13C-NMR; .delta.
(CH.sub.3OD), 177.4, 164.6, 153.3, 125.5, 54.1, 51.8, 46.2, 46.0,
39.6, 38.5, 38.3, 37.7, 34.5, 34.4, 33.9, 33.8, 26.4 and 22.0.
LRMS: +ve ion 359 [M+H], -ve ion 357 [M-1].
EXAMPLE 11
2R-Cyclopentylmethyl-3-(formyl-hydroxy-amino)-N-(1-methyl-1H-benzoimidazol-
-2-ylmethyl)-propionamide
##STR00019##
[0149] Example 11 was prepared in a similar manner to Example 1
using glycine in the place of t-leucine. The N-methyl substituent
was introduced on to the benzimidazole nitrogen using the procedure
detailed below.
2R-Cyclopentylmethyl-3-(formyl-hydroxy-amino)-N-(1-methyl-1H-benzoimidazol-
-2-ylmethyl)-propionamide
[0150] To a solution of
N-(1H-Benzoimidazol-2-ylmethyl)-2R-cyclopentylmethyl-3-(formyl-hydroxy-am-
ino)-propionamide (80 mg, 0.23 mmol) in anhydrous THF (7 ml) was
added triethylamine (30 .mu.l, 0.22 mmol) and iodomethane (14
.mu.l, 0.22 mmol). The reaction was stirred at 30.degree. C. for
approx. 3.5 hours. The material had not fully dissolved, so DMF was
added and the reaction stirred for a further 2 hours at 30.degree.
C. LRMS analysis showed presence of starting material, more
triethylamine (30 .mu.l, 0.22 mmol) and iodomethane (14 .mu.l, 0.22
mmol) were added and the reaction stirred at 30.degree. C. over
night. The solvent was removed in vacuo and the residue was
dissolved in DCM, washed with water, dried over anhydrous magnesium
sulfate and filtered. The solvent was removed in vacuo and the
crude mixture was purified by preparative HPLC to obtain the title
compound as a yellow oil. .sup.1H-NMR; .delta. (CH.sub.3OD), 8.31
(0.4H, s), 7.87 (0.6H, s), 7.58 (2H, m), 7.26 (2H, m), 4.89 (1H,
m), 4.55 (1H, m), 3.82 (1.2H, s), 3.81 (1.8H, s), 3.66 (2H, m),
2.93 (0.4H, m), 2.82 (0.6H, m), 1.63 (9H, m) and 1.09 (2H, m).
.sup.13C-NMR; .delta. (CH.sub.3OD), 177.2, 176.7, 164.6, 166.2,
130.6, 130.2, 128.2, 124.6, 124.1, 124.0, 123.9, 120.0, 119.4,
111.4, 54.1, 51.7, 46.1, 45.9, 39.6, 38.8, 38.4, 37.9, 37.6, 37.2,
34.4, 33.9, 30.8, 30.6 and 26.4. LRMS: +ve ion 359 [M+H], 381
[M+Na]. HPLC: RT=4.81 min.
EXAMPLE 12
3-Cyclopentyl-2R-[(formyl-hydroxy-amino)-methyl]-N-[1S-(1H-imidazol-2-yl)--
2,2-dimethyl-propyl]-propionamide
##STR00020##
[0152] .sup.1H-NMR; .delta. (CDCl.sub.3), 8.33 (0.6H, s), 7.86
(0.4H, s), 7.81 (0.4H, s), 7.14 (0.6H, s), 6.90 (2H, m), 5.15
(0.4H, d, J=9.6 Hz), 5.06 (0.6H, d, J=8.6 Hz), 4.00 (0.6H, m), 3.88
(0.4H, m), 3.65 (0.6H, m), 3.47 (0.4H, m), 3.19 (0.4H, m), 2.98
(0.6H, m), 1.56 (9H, m), 0.96 (6H, m), 0.95 (2H, m) and 0.77 (3H,
s). LRMS: +ve ion 351 [M+H], -ve ion 349 [M-H]. HPLC: RT=3.37
min.
[0153] The title compound was prepared from
2R-[(Benzyloxy-formylamino)-methyl]-hexanoic acid and
1S-(1H-Imidazol-2-yl)-2,2-dimethyl-propylamine by analogy with
Example 1. The preparation of
1S-(1H-Imidazol-2-yl)-2,2-dimethyl-propylamine is detailed below
(see Scheme 2)
##STR00021##
Step A:
[1S-(Methoxy-methyl-carbamoyl)-2,2-dimethyl-propyl]-carbamic acid
tert-butyl ester
[0154] To a solution of BOC protected t-leucine (30 g, 0.13 mol) in
DCM (400 ml) was added N,N-carbonyldiimidazole (63.3 g, 0.39 mol)
portionwise. Evolution of CO.sub.2 gas was observed and the
reaction allowed to stir for approx. 15 minutes before addition of
N,O-dimethylhydroxylamine hydrochloride (38 g, 0.39 mol). The
reaction was stirred overnight at ambient temperature. The solvent
was removed in vacuo and the residue dissolved in ethyl acetate,
washed with 1M hydrochloric acid, saturated sodium carbonate
solution and saturated sodium chloride solution, dried over
anhydrous magnesium sulfate and filtered. The solvent was removed
in vacuo to obtain a clear oil (26.5 g) that was purified by flash
chromatography (30% ethyl acetate/hexanes) when required.
[0155] .sup.1H-NMR; .delta. (CH.sub.3OD) 5.20 (1H, br s), 4.67 (1H,
d, J=9.5 Hz), 3.79 (3H, s), 3.20 (3H, s), 1.44 (9H, s) and 0.99
(9H, s).
Step B: (1S-Formyl-2,2-dimethyl-propyl)-carbamic acid tert-butyl
ester
[0156] To a stirred solution of
[1S-(Methoxy-methyl-carbamoyl)-2,2-dimethyl-propyl]-carbamic acid
tert-butyl ester (1.4 g, 5.11 mmol) in anhydrous THF (40 ml), under
a blanket of argon and in a dry ice/acetone bath, was added lithium
aluminium hydride. The reaction was stirred in the cooling bath for
approx. 1 hour, then allowed to warm to room temperature and stir
overnight. The reaction was cooled in an ice/water bath before
addition of ethyl acetate (4 ml), water (0.2 ml), 2.5M sodium
hydroxide (0.31 ml) and water (0.5 ml). The reaction mixture was
allowed to warm to room temperature and stir for approx. 45
minutes. The resulting semi-solid was filtered off, washed with
ethyl acetate and the filtrate concentrated in vacuo to obtain a
pale yellow oil (1.02 g, 92%). .sup.1H-NMR; .delta. (CDCl.sub.3)
9.84 (1H, s), 5.15 (1H, br s), 4.15 (1H, br s), 1.44 (9H, s) and
1.04 (9H, s).
Step C: [1S-(1H-Imidazol-2-yl)-2,2-dimethyl-propyl]-carbamic acid
tert-butyl ester
[0157] To a stirred solution of
(1S-Formyl-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester
(1.02 g, 4.75 mmol) in methanol (6 ml), was added 2M NH.sub.3 in
MeOH (11 ml, 21.8 mmol) and glyoxal trimer hydrate (499 mg, 2.37
mmol). The reaction was stirred at room temperature overnight, then
diluted with water and extracted with ethyl acetate. The organic
layer was washed with saturated sodium chloride solution, dried
over anhydrous magnesium sulfate and filtered. The solvent was
removed in vacuo to obtain a yellow oil (879 mg) that was purified
by flash chromatography (3-4% methanol/DCM) to yield a white solid
(495 mg, 95%). LRMS: +ve ion 254 [M+H], -ve ion 252 [M-1].
.sup.1H-NMR; .delta. (CDCl.sub.3) 6.92 (2H, s), 5.70 (1H, d, J=9.8
Hz), 4.65 (1H, d, J=9.7 Hz), 1.42 (9H, s) and 0.99 (9H, s).
Step D: 1S-(1H-Imidazol-2-yl)-2,2-dimethyl-propylamine
[0158] To a solution of
[1S-(1H-Imidazol-2-yl)-2,2-dimethyl-propyl]-carbamic acid
tert-butyl ester (495 mg, 1.95 mmol) in DCM (10 ml), was added TFA
(10 ml). The reaction was stirred at room temperature for approx. 4
hours. The solvent was removed in vacuo and the TFA co-evaporated
with toluene. The residue was dissolved in methanol and Amberlyst
A-21 ion exchange resin was added until pH 8 was obtained. The
resin was filtered off and the solvent removed in vacuo to obtain
the title compound as an oil (276 mg, 93%). LRMS: +ve ion 154
[M+H]. .sup.1H-NMR; .delta. (CH.sub.3OD) 7.01 (2H, s), 3.85 (1H, s)
and 0.96 (9H, s).
BIOLOGICAL EXAMPLE
[0159] The susceptibilities of two strains of bacteria to the
compounds of Example 1-4 were determined by a standard agar plate
dilution method following recommendations in British Society for
Antimicrobial Chemotherapy Working Party. 1991, "A guide to
sensitivity testing British Society for Antimicrobial Chemotherapy,
London, United Kingdom". Briefly, Iso-Sensitest agar (pH 7.2:
Oxoid, United Kingdom) is employed, supplemented with 5% horse
blood (Oxoid) and 20 .mu.g of NAD (Sigma) per ml are added to
support growth of fastidious bacteria. The inoculum used is
approximately 10.sup.4 colony forming units of each isolate
contained in a volume of 1 .mu.l. Plates are incubated 18 to 24 hr
in air, or for fasidious bacteria an atmosphere enriched with 4-6%
carbon dioxide at 35.degree. C. The MIC is determined as the lowest
concentration of an antimicrobial tested that inhibited growth of
the inoculum, disregarding a single persisting colony or faint haze
caused by the inoculation. The results were as follows:
TABLE-US-00002 S. aureus ATCC 29213 S. pneumoniae Example No MIC
.mu.g/ml ATCC 49619 MIC .mu.g/ml 1 4 2 2 8 2 3 8 2 4 8 4
* * * * *