Patent Application
20080242710
The present invention relates to tetrahydro-pyrrolo[1,2-b]isothiazole 1,1-dioxides which are pharmaceutically active, e.g. for use in the treatment of disorders mediated by interactions of LFA-1 with its ligands involved in cell adhesion, migration and activation.
Inflammatory recruitment of leukocytes is governed by dynamic interactions between integrins and endothelial immunoglobulin superfamily (IgSF) proteins, such as ICAM-1 (intercellular adhesion molecule-1), ICAM-2, ICAM-3 and the IgSF member junctional adhesion molecule 1 (JAM-1), all of which have been identified to be a ligand of the beta (2) integrin lymphocyte function-associated antigen 1 (LFA-1). Compounds which mediate, e.g. inhibit, interaction of LFA-1 and its ligands involved in cell adhesion, migration and activation have been found to constitute a therapeutic approach to inflammation and autoimmune diseases.
Now surprisigly it was found that 3a,4,5,6-tetrahydro-pyrrolo1,2-b]-isothiazoles wherein the sulphur is in the form of a dioxide mediate, e.g. inhibit, the activity of LFA-1 with its ligands involved in cell adhesion, migration and activation.
In one aspect the present invention provides the use of 3a,4,5,6-tetrahydro-pyrrolo1,2-b]-isothiazoles wherein the sulphur is in the form of a dioxide for the preparation of a medicament for use in the treatment or prevention of disorders, including diseases, mediated by interactions of LFA-1 with its ligands involved in cell adhesion, migration and activation.
In another aspect the present invention provides a 3a,4,5,6-tetrahydro-pyrrolo1,2-b]-isothiazole wherein the sulphur is in the form of a dioxide which is a compound of formula
such as a compound of formula
wherein
the dotted line is a bond or is no bond,
R1 is hydrogen, optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, aryl or heterocyclyl, hydroxy, SH, SR5, cyano, halogen or amino, or
the dotted line is no bond and R1 is attached to the ring system via a double bond and is oxo,
R2 is hydrogen or optionally substituted cycloalkyl, aryl, or heterocyclyl,
R3 is hydrogen, COOR6, aminocarbonyl, or optionally substituted alkyl, alkenyl, alkynyl, aralkyl, alkoxy, cycloalkyloxy, aryloxy, or heterocycyloxy,
R4 is hydrogen, halogen, hydroxy, SH, optionally substituted alkyl, alkenyl, alkynyl, alkoxy or alkylthio, or a silyl group such as trialkylsilyl or trialkylsilyloxy, e.g. tri(C1-6)alkylsilyl(oxy), N3, amino, or
R4 is heterocyclyl comprising at least one nitrogen atom as a heteroatom and being bound via that nitrogen atom to a compound of formula I, or
R4 is attached to the ring system by a double bond and is oxo; and
R5 and R6 independently of each other are alkyl, alkenyl, alkynyl, cycloalkyl, aryl or heterocyclyl,
In a compound of formula I preferably the dotted line is a bond, or is no bond, preferably the dotted line is a bond, and R1 is hydroxy, amino, (C1-8)alkyl, (C2-8)alkenyl, (C2-8alkynyl, (C1-8)alkoxy, e.g. including (C1-8)alkyl, (C2-8)alkenyl or (C1-8)alkoxy substituted by (C6-18)aryl, such as phenyl; or the dotted line is no bond and R1 is attached to the ring system via a double bond and is oxo, e.g.
the dotted line is a bond and R1 is hydroxy or (C1-8)alkoxy,
or the dotted line is a single bond and R1 is attached to the ring system via a double bond and is oxo.
In a compound of formula I preferably R2 is hydrogen, unsubstituted aryl, or substituted aryl, such as halophenyl, e.g. including dihalophenyl, such as 3,5-dihalophenyl, e.g. 3,5-dichlorophenyl, or hydrogen.
In a compound of formula I preferably R3 is optionally substituted alkyl, alkenyl, or alkynyl, e.g. of up to 8 carbon atoms, preferably substituted by aryl, such as substituted by substituted aryl, e.g. including (C6-18)aryl(C1-4)alkyl, e.g. phenyl(C1-4)alkyl; e.g. optionally substituted phenylmethyl, such as phenylmethyl, halophenylmethyl, e.g. bromophenylmethyl, cyanophenylmethyl, such as halophenylmethyl.
In a compound of formula I preferably R4 is hydroxy, a silyl group, such as tri(C1-6)alkylsilyloxy, e.g. (tert.butyl)(dimethyl)silyloxy, alkoxy, such as (C1-4)alkoxy, amino, or
R4 is heterocyclyl comprising at least one nitrogen atom as a heteroatom and being bound via that nitrogen atom to a compound of formula I, or
R4 is attached to the ring system by a double bond and is oxo;
such as hyxdroxy, (C1-4)alkoxy, tri(C1-6)alkylsilyloxy or oxo.
In another aspect the present invention provides a compound of formula I, which is a compound of formula
such as a compound of formula
wherein
The meanings of the residues in a compound provided by the present invention as defined herein include the following meanings:
Alkyl as a substituent or part of a substituent includes (C1-20)alkyl, such as (C1-8)alkyl, e.g. (C1-4)alkyl. Alkenyl as a substituent or part of a substituent includes (C2-20)alkenyl, such as (C2-8)alkenyl, Alkynyl as a substituent or part of a substituent includes (C2-20)alkynyl, such as (C2-8)alkynyl. Cycloalkyl as a substituent or part of a substituent includes saturated or partially unsaturated cycloalkyl, such as (C3-12)cycloalkyl.
Aryl as a substituent or part of a substituent includes (C6-18)aryl, such as phenyl, naphthyl. Heterocyclyl as a substituent or part of a substituent includes aliphatic heterocyclyl and aromatic heterocyclyl, having 3 to 8 ring members and 1 to 4 hetroatoms selected from N, O, S. Acyl includes alkylcarbonyl, cycloalkylcyrbonyl, arylcarbonyl or heterocyclylcarbonyl.
Alkoxy includes (C1-20)alkoxy, such as (C1-4)alkoxy.
Amino includes unsubstituted and substituted amino, e.g. including alkylamino, such as (C1-8)alkylamino, dialkylamino, such as (C1-8)dialkylamino, cycloalkylamino, such as (C3-12)cycloalkylamino, arylamino, e.g. including (C6-12)arylamino, acylamino, e.g. including (C2-18)acylamino, such as (C1-8)alkylcarbonylamino, (C6-12)arylcarbonylamino, (C3-12)cycloalkylcarbonylamino, and heterocyclylcarbonylamino; (acyl)(alkyl)-amino, such as ((C2-18)acyl)-((C1-4)alkyl))-amino, e.g. alkyl N-methyl-N-methylcarbonyl-amino, N-benzyl-N-methylcarbonyl-amino, N-ethyl-N-methylcarbonyl-amino, sulfonylamino, such as (C1-4)alkysulfonylamino, (C6-12)arylsulfonylamino, (C3-8)cyclohexylsulfonylamino, heterocycylsulfonylamino.
Substituted alkyl, alkenyl, alkynyl, alkoxy or alkylthio includes alkyl, alkenyl, alkynyl, alkoxy or alkylthio substituted by one or more halogen, hydroxy, SH, cyano, alkylthio, heterocyclyl, aryl, carboxyl, acyl, nitro, amino, alkoxy, carboxy, amido, or a silyl group, such as triakylsilyl or trialkylsilyloxy.
Substituted cycloalkyl, aryl or heterocyclyl or substituted cyclalkyloxy, heterocyclyloxy or aryloxy e.g. includes cycloalkyl, aryl or heterocyclyl, or cyclalkyloxy, heterocyclyloxy or aryloxy substituted by one or more alkyl, e.g. including haloalkyl, e.g. trifluoromethyl, cycloalkylalkyl, heterocyclyllalkyl, aralkyl, aryloxyalkyl, arylthioalkyl, arylsulfinylalkyl, alkenyl, such as arylalkenyl, heterocyclylalkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, e.g. including aminocarbonylaryl, oxo, hydroxy, SH, alkoxy, such as haloalkoxy, e.g. trifluoromethoxy, aryloxy, heterocyclyloxy, arylalkoxy, alkylthio, arylthio, heterocyclylthio, alkoxyarylthio, arylsulfinyl, alkylcarbonyloxy, arylcarbonyloxy, heterocyclylcarbonyloxy, alkylcarbonyl, alkoxycarbonyl, arylcarbonyl, aryloxycarbonyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, aminocarbonyl, e.g. including alkylaminocarbonyl, arylaminocarbonyl, sulfonaminocarbonyl, e.g. arylsulfonaminocarbonyl, halogen, nitro, cyano, amino, e.g. including alkylcarbonylamino, arylcarbonylamino, arylsulfonylamino; or triakylsilyl or trialkylsilyloxy.
Cycloalkyl, aryl and heterocyclyl substituents preferably include oxo, hydroxy, halogen, alkoxy, e.g. including (C1-4)alkoxy, N3, cyano, haloalkyl, e.g. including halo(C1-4)alkyl, heterocyclyl comprising 5 or 6 ring members and 1 to 4 heteroatoms selected from N, O, S, or optionally substituted amino.
Any ring defined herein, e.g. cycloalkyl, aryl or heterocyclyl, includes a single ring and a ring fused with another ring (system).
In another aspect the present invention provides a compound of anyone of Example 1 to Example 5, which are compounds of formula IEX.
The present invention includes a compound of formula I, wherein one, more or all of the residues defined have a preferred meaning as defined above, and the other residues have a meaning as defined above.
In a compound provided by the present invention each single defined substituent may be a preferred substituent, independently of the other substituents defined.
Compounds provided by the present invention are hereinafter designated as “compound(s) of (according to) the present invention”. 3a,4,5,6-Tetrahydro-pyrrolo1,2-b]-isothiazoles wherein the sulphur is in the form of a dioxide, include a compound of formula I and IPREF, and a compound of formula I and IPREF include a compound of formula IEX and I′EX. A compound of the present invention includes a compound in any form, e.g. in free form, in the form of a salt, in the form of a solvate and in the form of a salt and a solvate.
In another aspect the present invention provides a compound of the present invention in the form of a salt.
Such salts include preferably pharmaceutically acceptable salts, although pharmaceutically unacceptable salts are included, e.g. for preparation/isolation/purification purposes.
A salt of a compound of the present invention includes a metal salt or an acid addition salt. A compound of the present invention in free form may be converted into a corresponding compound in the form of a salt; and vice versa. A compound of the present invention in free form or in the form of a salt and in the form of a solvate may be converted into a corresponding compound in free form or in the form of a salt in non-solvated form; and vice versa.
A compound of the present invention and an intermediate of the present invention, may exist in the form of isomers and mixtures thereof; e.g. optical isomers, diastereoisomers, cis/trans conformers. A compound of the present invention and an intermediate of the present invention may e.g. contain asymmetric carbon atoms and may thus exist in the form of enantiomers or diastereoisomers and mixtures thereof, e.g. racemates. A compound of the present invention and an intermediate of the present invention may be present in the (R)—, (S)— or (R,S)-configuration preferably in the (R)- or (S)-configuration regarding substituents in specified positions in a compound of the present invention.
For example, a carbon atom in the pyrrolidine part of the ring system of a compound of the present invention, e.g. a compound of formula I, becomes an asymmetric carbon atom if a substitutent, other than hydrogen, is attached; and a compound of the present invention correspondingly substituted may be present in the (R)-, (S)- or (R,S)-configuration, preferably in the (R)- or (S)-configuration, regarding each of the substituents at such asymmetric carbon atom in a compound of the present invention, e.g. a compound of the present invention may be present in the (R)-, (S)- or (R,S)-configuration, preferably in the (R)- or (S)-configuration regarding R3, or R4.
Isomeric mixtures may be separated as appropriate, e.g. according, e.g. analogously, to a method as conventional, to obtain pure isomers. The present invention includes a compound of the present invention in any isomeric form and in any isomeric mixture.
The present invention also includes tautomers of a compound of the present invention, where tautomers can exist.
In another aspect the present invention provides a process for the production of a compound of formula I, comprising the steps
Further reaction e.g. includes replacing R1 and/or R4 in a compound of formula I obtained, to obtain a compound of formula I wherein R1 and/or R4 are different, e.g. by a method as appropriate, e.g. according, e.g. analogously, to a method as conventional.
A compound of formula I thus obtained may be converted into another compound of formula I, e.g. or a compound of formula I obtained in free form may be converted into a salt of a compound of formula I and vice versa.
A compound of formula II may be e.g. obtained by reacting a compound of formula
wherein R3 and R4 are as defined above, with a compound of formula
wherein R2 is as defined above in organic solvent in the presence of a base, e.g. potassium hydrogen carbonate.
A compound of formula III may be e.g. obtained by splitting off the N-protection group in a compound of formula
wherein R3 and R4 are as defined above, e.g. reacting a compound of formula V with tetrakis-(triphenylphosphine)-palladium in organic solvent in the presence of 1,4-diaza[2,2,2]bicyclooctane.
A compound of formula V may be e.g. obtained, if R4 in a compound of formula I is other than N3 or oxo, by reacting a compound of formula
wherein R3 is as defined above, with zinc powder in glacial acetic acid, to obtain a compound of formula
and optionally further reacting the amine group obtained, to obtain a compound of formula V, wherein R3 and R4 are as defined above, with the exception of R4 is oxo.
A compound of formula VI, wherein R3 is other than hydrogen, may be e.g. obtained by treating a compound of formula
with lithium-bis-trimethylsilylamide in organic solvent and treating the mixture obtained with a compound of formula
R3-Hal IX
wherein R3 is as defined above with the exception of hydrogen, and Hal is halogen, such as Br.
In any intermediate of formulae II, III, IV, V, VI, VII, VII or IX, functional groups, if present, optionally may be in protected form or in the form of a salt, if a salt-forming group is present. Protecting groups, optionally present, may be removed at an appropriate stage, e.g. according, e.g. analogously, to a method as conventional
Any compound described herein, e.g. a compound of the present invention and intermediates (starting materials) of formulae II, III, IV, V, VI, VII, VII or IX may be prepared as appropriate, e.g. according, e.g. analogously, to a method as conventional, e.g. or as specified herein.
The compounds of the present invention exhibit valuable pharmacological properties, e.g. by mediating, such as inhibiting the activity of LFA-1 interactions with its ligands, e.g. inhibiting the activity of LFA-1/ICAM-1, LFA-1/ICAM-2, LFA-1/ICAM-3 and/or LFA-1/JAM-1 interactions, e.g. LFA-1/ICAM-1 interaction, and thus mediating, e.g. inhibiting inflammation, e.g. as indicated in vitro and in vivo TEST SYSTEMS herein. The compounds of the present invention are therefore indicated for therapy.
The assay determines the binding of soluble human ICAM-1 to immobilized human LFA-1. LFA-1 is purified from JY cells, a human lymphoblastoid B cell-line, by immunoaffinity chromatography analogously as described by Dustin et al., J. Immunol. 148, 2654-2663, 1992. ICAM-1 mouse CK fusion protein (ICAM-1) is produced using the baculovirus system as described by Weitz-Schmidt et al., Anal. Biochem. 238, 184-190, 1996.
Purified LFA-1 is diluted 1:20 in phosphate buffered saline (PBS) containing 2 mM MgCl2, pH 7.4 and coated onto microtiter plates (Nunc) at 370 for 3 hours. Plates are blocked with 1% heat-treated bovine serum albumin in PBS for 2 hours at 370 followed by a washing step using PBS, 2 mM MgCl2, 1% fetal calf serum, pH 7.4 (assay buffer). Compounds of the present invention (10 mM solution in DMSO) are diluted in assay buffer and added to the plates. Biotinylated recombinant ICAM-1 in assay buffer (6 μg/ml) is added and allowed to bind at 370 for one hour. After incubation, wells are washed with assay buffer. Streptavidin-peroxidase diluted 1:5000 in assay buffer is added and incubated for 45 min at 370. Plates are washed with assay buffer and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt substrate solution is added to each well. The reaction is stopped after 20 minutes and bound ICAM-1 is determined by measuring the optical density at 405 nm in a microplate reader.
In this assay the compounds of the present invention exhibit activity, e.g. the compounds of the present invention inhibit adhesion of LFA-1 to ICAM.
Groups of 8 female NMRI mice are sensitized on the shaved abdomen with 50 μl of oxazolone (2% in acetone) and challenged with 10 μl of 0.2% oxazolone on the inner surface of the right ear 7 days later. The unchallenged left ears serve as normal controls and dermatitis is evaluated from the individual differences in auricular weights, which are taken as a measure of inflammatory swelling 24 hours after the challenge. The test groups are treated with the test compounds orally (2 hours after challenge), the controls are treated similarly with the vehicles alone. For oral administration the compounds are administered in an oil in H2O emulsion. Dermatitis is evaluated in test- and control groups. The animals are killed and both ears are cut off and weighed. Inhibitory activity of the test compounds is calculated from the differences in right and left ears (internal controls) in mice treated with test compounds compared with animals treated with the vehicle only. The data of the test- and the vehicle-treated control groups are statistically analyzed by ANOVA followed by Dunnet T-test (normal distribution or data) or by H and U-test, respectively. The compounds of the present invention inhibit the elicitation phase of allergic contact dermatitis based on the differences in auricular weights.
The compounds of the present invention are therefore indicated for use in the treatment or prevention of disorders, including diseases, mediated by interactions of LFA-1 with its ligands involved in cell adhesion, migration and activation.
Disorders, including diseases, mediated by interactions of LFA-1 with its ligands involved in cell adhesion, migration and activation include disorders associated with immune, inflammatory and allergic conditions, such as
Disorders Associated with Inflammation
Disorders Associated with Conditions of the Immune System,
Disorders Associated with Skin and Connective Tissue Conditions
Disorders Associated with Allergic Conditions,
Disorders Associated with Infectious Disorders, e.g. with Chronic Infectious Conditions,
Disorders Associated with Transplantation,
The compound of the present invention are preferably useful for treatment of disorders associated with conditions of the immune system, inflammation and transplantation; e.g. including psoriasis, rheumatoid arthritis, inflammatory bowel diseases (Crohn's disease, ulcerative colitis), (systemic) lupus erythematosus, multiple sclerosis, Sjoegren's syndrom, rejection after transplantation and graft vs. host disease and inflammatory skin diseases, e.g. dermatitis, such as atopic dermatitis, e.g. allergic contact dermatitis.
In one embodiment the compounds of the present invention are useful in the treatment of autoimmune diseases, e.g. rheumatoid arthritis, psoriasis, inflammatory bowel disease, (systemic) lupus erythematosus, multiple sclerosis or of inflammatory (skin) diseases, e.g. dermatitis;
more preferably in the treatment of inflammatory bowel disease or rheumatoid arthritis; e.g. or dermatitis.
In another aspect the present invention provides
For pharmaceutical use one or more compounds of the present invention may be used, e.g. one, or a combination of two or more compounds of the present invention, preferably one compound of the present invention is used.
A compound of the present invention may be used as a pharmaceutical in the form of a pharmaceutical composition.
In another aspect the present invention provides a pharmaceutical composition comprising a compound of the present invention in association with at least one pharmaceutically acceptable excipient, e.g. appropriate carrier and/or diluent, e.g. including fillers, binders, disintegrants, flow conditioners, lubricants, sugars or sweeteners, fragrances, preservatives, stabilizers, wetting agents and/or emulsifiers, solubilizers, salts for regulating osmotic pressure and/or buffers.
In another aspect the present invention provides
In a further aspect the present invention provides a method of treating disorders which are mediated by interactions of LFA-1 with its ligands involved in cell adhesion, migration and activation, which treatment comprises administering to a subject in need of such treatment a therapeutically effective amount of a compound of the present invention; e.g. in the form of a pharmaceutical composition.
In another aspect the present invention provides
A compound of the present invention for the manufacture of a medicament,
The use of a compound of the present invention for the manufacture of a medicament,
e.g. a pharmaceutical composition,
for the treatment of disorders, which are mediated by interactions of LFA-1 with its ligands involved in cell adhesion, migration and activation.
Treatment of disorders (diseases) as used herein includes treatment and prophylaxis (prevention).
For such treatment, the appropriate dosage will, of course, vary depending upon, for example, the chemical nature and the pharmacokinetic data of a compound of the present invention used, the individual host, the mode of administration and the nature and severity of the conditions being treated. However, in general, for satisfactory results in larger mammals, for example humans, an indicated daily dosage includes a range
A compound of the present invention may be administered to larger mammals, for example humans, by similar modes of administration than conventionally used with other mediators, e.g. low molecular weight inhibitors, of activity of LFA-1 with its ligands involved in cell adhesion, migration and activation.
A compound of the present invention may be administered by any route, e.g. by any conventional route, for example enterally, e.g. including nasal, buccal, rectal, oral, administration; parenterally, e.g. including intravenous, intraarterial, intramuscular, intracardiac, subcutanous, intraosseous infusion, transdermal (diffusion through the intact skin), transmucosal (diffusion through a mucous membrane), inhalational administration; topically; e.g. including epicutaneous, intranasal, intratracheal administration; intraperitoneal (infusion or injection into the peritoneal cavity); epidural (peridural) (injection or infusion into the epidural space); intrathecal (injection or infusion into the cerebrospinal fluid); intravitreal (administration via the eye); or via medical devices, e.g. for local delivery, e.g. stents, e.g. in form of coated or uncoated tablets, capsules, (injectable) solutions, infusion solutions, solid solutions, suspensions, dispersions, solid dispersions; e.g. in the form of ampoules, vials, in the form of creams, gels, pastes, inhaler powder, foams, tinctures, lip sticks, drops, sprays, or in the form of suppositories.
For topical use, e.g. including administration to the eye, satisfactory results may be obtained with local administration of a 0.5-10%, such as 1-3% concentration of active substance several times daily, e.g. 2 to 5 times daily.
The compounds of the present invention may be administered in the form of a pharmaceutically acceptable salt, or in free form; optionally in the form of a solvate. A compound of the present invention in the form of a salt and/or in the form of a solvate exhibit the same order of activity as a compound of the present invention in free form.
A compound of the present invention may be used for any method or use as described herein alone or in combination with one or more, at least one, other, second drug substance.
In another aspect the present invention provides
Combinations include fixed combinations, in which a compound of the present invention and at least one second drug substance are in the same formulation; kits, in which a compound of the present invention and at least one second drug substance in separate formulations are provided in the same package, e.g. with instruction for co-administration; and free combinations in which a compound of the present invention and at least one second drug substance are packaged separately, but instruction for concomitant or sequential administration are given.
In another aspect the present invention provides
Treatment with combinations according to the present invention may provide improvements compared with single treatment.
In another aspect the present invention provides
A combination of the present invention and a second drug substance as a combination partner may be administered by any conventional route, for example as set out above for a compound of the present invention. A second drug may be administered in dosages as appropriate, e.g. in dosage ranges which are similar to those used for single treatment, or, e.g. in case of synergy, even below conventional dosage ranges.
Pharmaceutical compositions according to the present invention may be manufactured according, e.g. analogously, to a method as conventional, e.g. by mixing, granulating, coating, dissolving or lyophilizing processes. Unit dosage forms may contain, for example, from about 0.1 mg to about 1500 mg, such as 1 mg to about 1000 mg.
Pharmaceutical compositions comprising a combination of the present invention and pharmaceutical compositions comprising a second drug as described herein, may be provided as appropriate, e.g. according, e.g. analogously, to a method as conventional, or as described herein for a pharmaceutical composition of the present invention.
By the term “second drug substance” is meant a chemotherapeutic drug, especially any chemotherapeutic agent other than a compound of the present invention, such as a compound of formula I.
For example, a second drug substance as used herein includes e.g.
Anti-inflammatory and/or immunomodulatory drugs which are prone to be useful in combination with a compound of the present invention include e.g.
and rapamycin derivatives, e.g. including
40-O-alkyl-rapamycin derivatives, such as 40-O-hydroxyalkyl-rapamycin derivatives, such as 40-O-(2-hydroxy)-ethyl-rapamycin (everolimus),
32-deoxo-rapamycin derivatives and 32-hydroxy-rapamycin derivatives, such as 32-deoxorapamycin,
16-O-substituted rapamycin derivatives such as 16-pent-2-ynyloxy-32-deoxorapamycin,
16-pent-2-ynyloxy-32 (S or R)-dihydro-rapamycin, 16-pent-2-ynyloxy-32(S or R)-dihydro-40-O-(2-hydroxyethyl)-rapamycin,
rapamycin derivatives which are acylated at the oxygen group in position 40, e.g. 40-[3-hydroxy-2-(hydroxy-methyl)-2-methylpropanoate]-rapamycin (also known as CCl779), rapamycin derivatives which are substituted in 40 position by heterocyclyl, e.g. 40-epi-(tetrazolyl)-rapamycin (also known as ABT578),
the so-called rapalogs, e.g. as disclosed in WO9802441, WO0114387 and WO0364383, such as AP23573, and
compounds disclosed under the name TAFA-93 AP23464, AP23675, AP23841 and biolimus (e.g. biolimus A9).
Anti-inflammatory which are prone to be useful in combination with a compound of the present invention include e.g. non-steroidal antiinflammatory agents (NSAIDS) such as propionic acid derivatives (alminoprofen, benoxaprofen, bucloxic acid, carprofen, fenbufen, fenoprofen, fluprofen, flurbiprofen, ibuprofen, indoprofen, ketoprofen, miroprofen, naproxen, oxaprozin, pirprofen, pranoprofen, suprofen, tiaprofenic acid, and tioxaprofen), acetic acid derivatives (indomethacin, acemetacin, alclofenac, clidanac, diclofenac, fenclofenac, fenclozic acid, fentiazac, furofenac, ibufenac, isoxepac, oxpinac, sulindac, tiopinac, tolmetin, zidometacin, and zomepirac), fenamic acid derivatives (flufenamic acid, meclofenamic acid, mefenamic acid, niflumic acid and tolfenamic acid), biphenylcarboxylic acid derivatives (diflunisal and flufenisal), oxicams (isoxicam, piroxicam, sudoxicam and tenoxican), salicylates (acetyl salicylic acid, sulfasalazine) and the pyrazolones (apazone, bezpiperylon, feprazone, mofebutazone, oxyphenbutazone, phenylbutazone); cyclooxygenase-2 (COX-2) inhibitors such as celecoxib; inhibitors of phosphodiesterase type IV (PDE-IV); antagonists of the chemokine receptors, especially CCR-1, CCR-2, and CCR-3; cholesterol lowering agents such as HMG-CoA reductase inhibitors (lovastatin, simvastatin and pravastatin, fluvastatin, atorvastatin, and other statins), sequestrants (cholestyramine and colestipol), nicotinic acid, fenofibric acid derivatives (gemfibrozil, clofibrat, fenofibrate and benzafibrate), and probucol; anticholinergic agents such as muscarinic antagonists (ipratropium bromide); other compounds such as theophylline, sulfasalazine and aminosalicylates, e.g. 5-aminosalicylic acid and prodrugs thereof, antirheumatics.
Antiallergic drugs which are prone to be useful in combination with a compound of the present invention include e.g. antihistamines (H1-histamine antagonists), e.g. bromopheniramine, chlorpheniramine, dexchlorpheniramine, triprolidine, clemastine, diphenhydramine, diphenylpyraline, tripelennamine, hydroxyzine, methdilazine, promethazine, trimeprazine, azatadine, cyproheptadine, antazoline, pheniramine pyrilamine, astemizole, terfenadine, loratadine, cetirizine, fexofenadine, descarboethoxyloratadine, and non-steroidal anti-asthmatics such as β2-agonists (terbutaline, metaproterenol, fenoterol, isoetharine, albuterol, bitolterol, salmeterol and pirbuterol), theophylline, cromolyn sodium, atropine, ipratropium bromide, leukotriene antagonists (zafirlukast, montelukast, pranlukast, iralukast, pobilukast, SKB-106,203), leukotriene biosynthesis inhibitors (zileuton, BAY-1005); bronchodilators, antiasthmatics (mast cell stabilizers).
The weight ratio of a compound of the present invention to other drug may vary, e.g. dependent on the activity of the combination partners used, the kind of disease treated, and will further depend upon the effective dose of each ingredient and may be established e.g. by instructions given for the other drug and testing, e.g. according, e.g. analogously, to a method as conventional.
The chemical names of the compounds of the present invention as indicated herein are copied from ISIS, version 2.5 (AutoNom 2000 Name).
In the following Examples all temperatures indicated are in degree Celsius (° C.). The following abbreviations are used:
EtOAc ethyl acetate
rt room temperature
THF tetrahydrofurane
To a solution of 20 g of (2S,4S)-4-azido-pyrrolidine-1,2-dicarboxylic acid 1-allyl ester 2-methyl ester and 14.85 g imidazole in 300 ml of CH3CN are added 26.3 g of (tert.butyl)(dimethyl)silylchloride in one portion and the mixture obtained is stirred for 1 hour at rt. To the mixture obtained EtOAc and half saturated aqueous NaCl solution are added, the phase obtained are separated, the organic layer obtained is washed, dried and from, the mixture obtained solvent is evaporated. The evaopration residue obtained is subjected to chromatography. (2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-allyl ester 2-methyl ester is obtained in the form of a colorless oil.
MS: 366/709 (MNa+/2MNa+), 1H-NMR and 13C-NMR data are in accordance with the proposed structure.
To a solution of 10 g of (2S,4R)-4-(tert.butyl)(dimethyl)silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-allyl ester 2-methyl ester and 14.55 g of 4-bromobenzylbromide in 100 ml of THF are added 11.61 g of solid potassium hexamethyl disilazane in such a rate that the temperature is kept below 40°. The mixture obtained is stirred at rt for 20 minutes and 1N aqueous HCl and EtOAc are added. The phases obtained are separated and the organic layer obtained is washed, dried and solvent is evaporated. The evaporation resisue obtained is subjected to chromatography. (2S,4R)-2-(4-Bromo-benzyl)-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-allyl ester 2-methyl ester, (3.3 g) and (2R,4R)-2-(4-Bromo-benzyl)-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-allyl ester 2-methyl ester (9.1 g) are obtained. Both compounds: MS: 535/1047 (MNa+/2MNa+); 1H-NMR and 13C-NMR data are in accordance with the proposed structure.
A mixture of 2.81 g of compound (2S,4R)-2-(4-bromo-benzyl)-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-allyl ester 2-methyl ester, 3.24 g of 1,4-diaza-bicyclo[2.2.2]octane and 653 mg of tetrakis-(triphenylphosphine)-palladium in 30 ml of CH2Cl2 is stirred at rt for 25 minutes. EtOAc and an aqueous, saturated NaHCO3 solution are added, The phases obtained are separated, the organic layer obtained is dried and solvent is evaporated. The evaporation residue obtained is subjected to chromatograph. (2S,4R)-2-(4-Bromo-benzyl)-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-2-carboxylic acid methyl ester is obtained in the form of an oil.
MS:: 451 (MNa+), 1H-NMR and 13C-NMR data are in accordance with the proposed structure.
A Compound of Formula
To a solution of 400 mg of (2S,4R)-2-(4-bromo-benzyl)-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-2-carboxylic acid methyl ester and 1.5 g of 4-dimethylamino pyridine (DMAP, Steglich base) in 20 ml of CH3CN are added 600 mg of 2,5-dichlorophenyl methanesulfonyl chloride at rt and the mixture obtained is stirred at rt. To the mixture obtained EtOAc and a saturated aqueous NAHCO3-solution is added, the phases obtained are separated and the organic layer is washed, dried, and solvent is evaporated. The evaporation residue obtained is subjected to chromatography. (2S,4R)-2-(4-Bromo-benzyl)-4-(tert-butyl-dimethyl-silanyloxy)-1-(3,5-dichloro-phenylmethanesulfonyl)-pyrrolidine-2-carboxylic acid methyl ester is obtained in the form of a slightly yellow oil.
MS:: 673 (MNa+), 1H-NMR and 13C-NMR data are in accordance with the proposed structure.
A Compound of Formula
To a solution of 460 mg of (2S,4R)-2-(4-bromo-benzyl)-4-(tert-butyl-dimethyl-silanyloxy)-1-(3,5-dichloro-phenylmethanesulfonyl)-pyrrolidine-2-carboxylic acid methyl ester in 15 ml of THF are added 222 mg of solid potassium hexamethyl disilazane in one portion at rt. The mixture obtained is stirred for 15 minutes at rt and EtOAc and 1N HCl are added. The phases obtained are separated, the organic layer obtained is washed, dried and solvent is evaporated. (3aS,5R)-3a-(4-Bromo-benzyl)-5-(tert-butyl-dimethyl-silanyloxy)-2-(3,5-dichloro-phenyl)-1,1-dioxo-3a,4,5,6-tetrahydro-1H-1 lambda*6*-pyrrolo[1,2-b]isothiazol-3-ol is obtained in the form of a crystalline solid.
MS, 1H-NMR and 13C-NMR data are in accordance with the proposed structure.
A Compound of Formula
An approx. 1M solution of diazomethane in diethylether is added to a solution of 410 mg of (3aS,5R)-3a-(4-bromo-benzyl)-5-(tert-butyl-dimethyl-silanyloxy)-2-(3,5-dichloro-phenyl)-1,1-dioxo-3a,4,5,6-tetrahydro-1H-1lambda*6*-pyrrolo[1,2-b]isothiazol-3-ol in 20 ml of EtOAc until the characteristic yellow color of diazomethane does not longer disappear. From the mixture obtained solvent is evaporated and the evaporation residue is subceted to chromatography. (3aS,5R)-3a-(4-Bromo-benzyl)-5-(tert-butyl-dimethyl-silanyloxy)-2-(3,5-dichloro-phenyl)-3-methoxy-3a,4,5,6-tetrahydro-pyrrolo[1,2-b]isothiazole 1,1-dioxide is obtained in the form of an amorphous powder.
MS:: 654 (MNa+), 1H-NMR and 13C-NMR data are in accordance with the proposed structure.
A Compound of Formula
To a solution of 280 mg of (3aS,5R)-3a-(4-bromo-benzyl)-5-(tert-butyl-dimethyl-silanyloxy)-2-(3,5-dichloro-phenyl)-3-methoxy-3a,4,5,6-tetrahydro-pyrrolo[1,2-b]isothiazole 1,1-dioxide in 8 ml of CH3CN are added 3 ml of aqueous (40 v/v %) hydrogen fluoride solution and the mixture obtained is stirred for 70 minutes at rt. To the mixture obtained EtOAc and an aqueous solution of saturated NaHCO3 are added and the phases obtained are separated. The organic layer obtained is washed, dried and solvent is evaporated. The evaporation residue obtained is subjected to chromatography. (3aS,5R)-3a-(4-Bromo-benzyl)-2-(3,5-dichloro-phenyl)-3-methoxy-1,1-dioxo-3a,4,5,6-tetrahydro-1H-1lambda*6*-pyrrolo[1,2-b]isothiazol-5-ol is obtained in the form of an amorphous powder.
MS: 530/1055 (MNa+/2MNa+), 1H-NMR and 13C-NMR data of any compound described are in accordance with the proposed structure:
A Compound of Formula
A mixture of 83 mg of 1-hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide (IBX, CAS Regno: 444722-55-8) and 50 mg of (3aS,5R)-3a-(4-bromo-benzyl)-2-(3,5-dichloro-phenyl)-3-methoxy-1,1-dioxo-3a,4,5,6-tetrahydro-1H-1lambda*6*-pyrrolo[1,2-b]isothiazol-5-ol in 5 ml EtOAc are reacted under microwave conditions (1000; 65 minutes; Personal chemistry Emrys optimizer). The mixture obtained is filtrated (removal of excess reagent), the filtrate obtained is concentrated at reduced pressure and the concentration residue obtained is subjected to chromatography. (S)-3a-(4-Bromo-benzyl)-2-(3,5-dichloro-phenyl)-3-methoxy-1,1-dioxo-3a,4-dihydro-1H-1 lambda*6*-pyrrolo[1,2-b]isothiazol-5-one is obtained in the form of an amorphous solid.
MS: 537 (MNa+), 1H-NMR and 13C-NMR data of any compound described are in accordance with the proposed structure.
According to a method as set out in any of the previous Examples the compound of formula
is obtained. MS, 1H-NMR and 13C-NMR data are in accordance with the proposed structure.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0520378.1 | Oct 2005 | GB | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP06/67017 | 10/4/2006 | WO | 00 | 4/3/2008 |
