1-aryl-dibenzothiophenes

BACKGROUND OF THE INVENTION
The prevalence of insulin resistance in glucose intolerant subjects has long been recognized. Reaven et al (American Journal of Medicine 1976, 60, 80) used a continuous infusion of glucose and insulin (insulin/glucose clamp technique) and oral glucose tolerance tests to demonstrate that insulin resistance existed in a diverse group of nonobese, nonketotic subjects. These subjects ranged from borderline glucose tolerant to overt, fasting hyperglycemia. The diabetic groups in these studies included both insulin dependent (IDDM) and noninsulin dependent (NIDDM) subjects.
Coincident with sustained insulin resistance is the more easily determined hyperinsulinernia, which can be measured by accurate determination of circulating plasma insulin concentration in the plasma of subjects. Hyperinsulinemia can be present as a result of insulin resistance, such as is in obese and/or diabetic (NIDDM) subjects and/or glucose intolerant subjects, or in IDDM subjects, as a consequence of over injection of insulin compared with normal physiological release of the hormone by the endocrine pancreas.
The association of hyperinsulinemia with obesity and with ischemic diseases of the large blood vessels (e.g. atherosclerosis) has been well established by numerous experimental, clinical and epidemiological studies (summarized by Stout, Metabolism 1985, 34, 7, and in more detail by Pyorala et al, Diabetes/Metabolism Reviews 1987, 3, 463). Statistically significant plasma insulin elevations at 1 and 2 hours after oral glucose load correlates with an increased risk of coronary heart disease.
Since most of these studies actually excluded diabetic subjects, data relating the risk of atherosclerotic diseases to the diabetic condition are not as numerous, but point in the same direction as for nondiabetic subjects (Pyorala et al). However, the incidence of atherosclerotic diseases in morbidity and mortality statistics in the diabetic population exceeds that of the nondiabetic population (Pyorala et al; Jarrett Diabetes/Metabolism Reviews 1989,5, 547; Harris et al, Mortality from diabetes, in Diabetes in America 1985).
The independent risk factors obesity and hypertension for atherosclerotic diseases are also associated with insulin resistance. Using a combination of insulin/glucose clamps, tracer glucose infusion and indirect calorimetry, it has been demonstrated that the insulin resistance of essential hypertension is located in peripheral tissues (principally muscle) and correlates directly with the severity of hypertension (DeFronzo and Ferrannini, Diabetes Care 1991, 14, 173). In hypertension of the obese, insulin resistance generates hyperinsulinemia, which is recruited as a mechanism to limit further weight gain via thermogenesis, but insulin also increases renal sodium reabsorption and stimulates the sympathetic nervous system in kidneys, heart, and vasculature, creating hypertension.
It is now appreciated that insulin resistance is usually the result of a defect in the insulin receptor signaling system, at a site post binding of insulin to the receptor. Accumulated scientific evidence demonstrating insulin resistance in the major tissues which respond to insulin (muscle, liver, adipose), strongly suggests that a defect in insulin signal transduction resides at an early step in this cascade, specifically at the insulin receptor kinase activity, which appears to be diminished (reviewed by Haring, Diabetalogia 1991, 34, 848).
Protein-tyrosine phosphatases (PTPases) play an important role in the regulation of phosphorylation of proteins. The interaction of insulin with its receptor leads to phosphorylation of certain tyrosine molecules within the receptor protein, thus activating the receptor kinase. PTPases dephosphorylate the activated insulin receptor, attenuating the tyrosine kinase activity. PTPases can also modulate post-receptor signaling by catalyzing the dephosphorylation of cellular substrates of the insulin receptor kinase. The enzymes that appear most likely to closely associate with the insulin receptor and therefore, most likely to regulate the insulin receptor kinase activity, include PTP1B, LAR, PTP.alpha. and SH-PTP2 (B. J. Goldstein, J. Cellular Biochemistry 1992, 48, 33; B. J. Goldstein, Receptor 1993, 3, 1-15,; F. Ahmad and B. J. Goldstein Biochim. Biophys Acta 1995, 1248, 57-69).
McGuire et al. (Diabetes 1991, 40, 939), demonstrated that nondiabetic glucose intolerant subjects possessed significantly elevated levels of PTPase activity in muscle tissue vs. normal subjects, and that insulin infusion failed to suppress PTPase activity as it did in insulin sensitive subjects.
Meyerovitch et al (J. Clinical Invest. 1989, 84, 976) observed significantly increased PTPase activity in the livers of two rodent models of IDDM, the genetically diabetic BB rat, and the STZ-induced diabetic rat. Sredy et al (Metabolism, 44, 1074, 1995) observed similar increased PTPase activity in the livers of obese, diabetic ob/ob mice, a genetic rodent model of NIDDM.
The compounds of this invention have been shown to inhibit PTPases derived from rat liver microsomes and human-derived recombinant PTPase-1B (hPTP-1B) in vitro. They are useful in the treatment of insulin resistance associated with obesity, glucose intolerance, diabetes mellitus, hypertension and ischemic diseases of the large and small blood vessels.
T. Kimura and N. Furukawa Tet. Lett. 1995, 36, 1079-1080, disclosed one example of a 1-aryl-dibenzothiophene shown as compound A (R=Me, R'=SPh). This compound was prepared for use in a chemical photolysis study. E. V. Brown and R. Isbrandt J. Med. Chem. 1971, 14, 84-85, disclosed one example of a 1-aryl-dibenzothiophene shown as compound A (R=NMe.sub.2, R'=H). This compound was prepared for use in a carcinogenicity study where it was found to be inactive. Neither of the examples in these articles contained the appropriate substitution on the 1-phenyl group necessary for in vitro PTPase inhibition activity. The synthetic process to prepare the two examples represented by compounds A was different to the processes used to prepare the 1-aryl-dibenzothiophenes of this invention. ##STR2##
DESCRIPTION OF THE INVENTION
This invention provides compounds of Formula I having the structure ##STR3## wherein: B and D are each, independently, hydrogen, halogen, --CN, alkyl of 1-6 carbon atoms, aryl, or aralkyl of 6-12 carbon atoms;
X is H, or halogen;
R.sup.1 is hydrogen, alkyl of 1-6 carbon atoms, --CH(R.sup.2)W, --C(CH.sub.3).sub.2 CO.sub.2 R.sup.3, 5-thiazolidine-2,4-dione, --CH(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3, --COR.sup.3, or --PO.sub.3 (R.sup.3).sub.2 ;
R.sup.2 is hydrogen, alkyl of 1-6 carbon atoms, aralkyl of 6-12 carbon atoms, aryl, --CH.sub.2 (1H-imidazol-4-yl), --CH.sub.2 (3-1H-indolyl), --CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), --CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), or --CH.sub.2 (3-pyridyl);
W is --CO.sub.2 R.sup.3, --CONH.sub.2, --CONHOH, --CN, --CONH(CH.sub.2).sub.2 CN, 5-tetrazole, or --PO.sub.3 (R.sup.3).sub.2 ;
R.sup.3 is hydrogen, alkyl of 1-6 carbon atoms, or aryl;
R.sup.4 is hydrogen, or alkyl of 1-6 carbon atoms;
n is 0-2;
or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.
Pharmaceutically acceptable salts can be formed from organic and inorganic acids, for example, acetic, propionic, lactic, citric, tartaric, succinic, fumaric, maleic, malonic, mandelic, malic, phthalic, hydrochloric, hydrobromic, phosphoric, nitric, sulfuric, methanesulfonic, napthalenesulfonic, benzenesulfonic, toluenesulfonic, camphorsulfonic, and similarly known acceptable acids when a compound of this invention contains a basic moiety, such as when R.sup.2 is --CH.sub.2 (3-pyridyl) or contains similar basic moieties. Salts may also be formed from organic and inorganic bases, preferably alkali metal salts, for example, sodium, lithium, or potassium, when a compound of this invention contains a carboxylate or phenolic moiety.
Alkyl includes both straight chain as well as branched moieties. Halogen means bromine, chlorine, fluorine, and iodine. It is preferred that the aryl portion of the aryl or aralkyl substituent is a phenyl or naphthyl; with phenyl being most preferred. The aryl moiety may be optionally mono-, di-, or tri-substituted with a substituent selected from the group consisting of alkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, trifluoromethyl, halogen, alkoxycarbonyl of 2-7 carbon atoms, alkylamino of 1-6 carbon atoms, and dialkylamino in which each of the alkyl groups is of 1-6 carbon atoms, nitro, cyano, --CO.sub.2 H, alkylcarbonyloxy of 2-7 carbon atoms, and alkylcarbonyl of 2-7 carbon atoms.
The compounds of this invention may contain an asymmetric carbon atom and some of the compounds of this invention may contain one or more asymmetric centers and may thus give rise to optical isomers and diastereomers. While shown without respect to stereochemistry in Formula I, the present invention includes such optical isomers and diastereomers; as well as the racemic and resolved, enantiomerically pure R and S stereoisomers; as well as other mixtures of the R and S stereoisomers and pharmaceutically acceptable salts thereof.
The compounds of this invention may be atropisomers by virtue of possible restricted or slow rotation about the aryl-tricyclic single bond. This restricted rotation creates additional chirality and leads to enantiomeric forms. If there is an additional chiral center in the molecule, diasteriomers exist and can be seen in the NMR and via other analytical techniques. While shown without respect to atropisomer stereochemistry in Formula I, the present invention includes such atoropisomers (enantiomers and diastereomers; as well as the racemic, resolved, pure diastereomers and mixtures of diastereomers) and pharmaceutically acceptable salts thereof.
Preferred compounds are those in which n=0; and those in which n=0, and B and D are each, independently, hydrogen or halogen. More preferred compounds of this invention are:
(R)-2-[2,6-dibromo-4-(2-bromo-dibenzothiophen-1-yl)-phenoxy]-3-phenyl-propionic acid;
(R)-2-[2,6-dibromo-4-(dibenzothiophen-1-yl)-phenoxy]-3-phenyl-propionic acid; and
(R)-2-[2,6-dibromo-4-(2-bromo-dibenzothiophen-1-yl)-phenoxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid
The compounds of this invention can be prepared according to the following schemes from commercially available starting materials or starting materials which can be prepared using literature procedures. These schemes show the preparation of representative compounds of this invention. ##STR4##
In Scheme 1, commercially available thianaphthene (II) is treated with one to 1.3 molar equivalents of an alkyl lithium reagent such as N-butyl lithium most preferably in a nonprotic solvent such as THF at temperatures ranging from -78.degree. C. to room temperature under an inert atmosphere such as nitrogen or argon to provide the 2-lithiated-thiophene derivative. This lithiated analog is reacted in situ with one or more molar equivalents of allyl bromide, generally at -78.degree. C. to room temperature for 5 min to 3 h to provide the compound of formula (III).
The compounds of formula (III) can be acylated with one or more molar equivalents of a commercially available p-anisoyl acid chloride of formula (IV:, B, D is H) to produce the acylated derivative of formula (V: B, D is H). This acylation is accomplished most readily using a one to five molar equivalents of a Lewis acid catalyst such as tin tetrachloride or aluminum chloride in an inert solvent such as dichloromethane, 1,2-dichloroethane or carbon disulfide, generally at temperatures such as -78.degree. C. to room temperature.
Cyclization of the compounds of formula (V: B, D is H) is generally best accomplished using one to ten molar equivalents of a strong Lewis acid such as a trihaloborane, most conveniently tribromoborane. The reaction is best performed at -78.degree. C. with warming to room temperature in a halocarbon solvent such as dichloromethane under an inert atmosphere such as nitrogen or argon. These procedures not only effect cyclization and aromatization with concomitant loss of water, but also result in demethylation of any pendant methoxy moieties and result in the production of compounds of formula (Ia: B, D is H).
In an analogous fashion to the reactions above in Scheme 1, the compounds of formula (Ia: B, D is lower alkyl) can be prepared starting from the compound of formula (III) and the appropriate benzoic acid chloride (IV: B, D is lower alkyl). The benzoic acid chloride (IV: B, D is lower alkyl) is prepared from the corresponding benzoic acid by standard procedures using reagents such as oxalyl chloride and thionyl chloride. The starting benzoic acid of the benzoic acid chloride (IV: B, D is lower alkyl) is commercially available or can be easily prepared by known procedures. For example, the acid starting material for benzoic acid chloride (IV: B, D is isopropyl) can be prepared using a modification of the method of Schuster, et al., J. Org. Chem. 1988, 53, 5819. Thus commercially available 2,6-diisopropyl phenol is brominated in the 4-position (bromine/acetic acid), methylated (iodomethane/potassium carbonate/DMF), reacted with n-butyl lithium to effect lithium halogen exchange and the resultant organolithium species is reacted with carbon dioxide to provide 3,5-diisopropyl, 4-methoxy benzoic acid. ##STR5##
Further derivatives of the compounds of formula (I) in Scheme 2 can be prepared by the following methods. The phenol of formula (Ib: R.sup.1 is H) (Scheme 2) can be conveniently iodinated to the diiodophenol of formula (Ic: B, D is I; R.sup.1 is H) using at least two molar equivalents of iodine in the presence of two or more molar equivalents of an alkali metal hydroxide such as NaOH in a alcohol solvent such as methanol at -20.degree. C. to room temperature. Similarly the monoiodophenol (Ic: B is I; R.sup.1, D is H) can be prepared from the phenol of formula (Ib: R.sup.1 is H) (Scheme 2) using one to 1.5 molar equivalents of iodine in the presence of at least one equivalent of an alkali metal hydroxide such as NaOH in a alcohol solvent such as methanol at -20.degree. C. to room temperature. Either the monoiodophenol (Ic: B is I; R.sup.1, D is H) or the diiodophenol (Ic: B, D is I; R.sup.1 is H) can be converted to the respective methyl ether derivative of formula (Ic: B, D is I; R.sup.1 is Me) or (Ic: B is I; D is H, R.sup.1 is Me) by reacting the phenol moiety with a suitable methylating agent such as one or more molar equivalents of methyl iodide or dimethylsulfate employing a base such an alkali methyl carbonate or hydroxide such as potassium carbonate or sodium hydroxide in a suitable solvent such as THF, DMF or DMSO. The reaction is generally performed at temperatures ranging from 0.degree. C. to 60.degree. C.
The monoiodo methylether derivative of formula (Ic: B is I; D is H, R.sup.1 is Me) or the diiodo methylether of formula (Ic: B, D is I; R.sup.1 is Me) can be reacted with one or more molar equivalents of copper (I) cyanide for the monoiodo analog or two or more molar equivalents of copper (I) cyanide for the diiodo derivative to produce the monocyanomethyl ether of formula (Ic: B is CN; D is H; R.sup.1 is Me) or the dicyanomethyl ether of formula Ic: B, D is CN; R.sup.1 is Me). The cyanation reaction is generally performed at temperatures ranging from 100.degree. C. to 250.degree. C. employing polar aprotic solvents such as DMF, 1-methyl-2-pyrrolidinone or HMPA. Quinoline or pyridine can also be used. The mono or dicyano methoxy analogs of formula (Ic: B is CN; D is H or CN; R.sup.1 is Me) can be converted to the corresponding mono or dicyano phenol analogs of formula (Ic: B is CN; D is H or CN; R.sup.1 is H) (Scheme 2) using standard demethylation procedures including one or more molar equivalents of boron tribromide or boron trichloride in dichloromethane at -78.degree. C. to room temperature; excess neat pyridinium hydrochloride at 190 to 280.degree. C.; hydrobromic acid in acetic acid at 0.degree. C. to 50.degree. C.; excess trimethylsilylbromide or trimethylsilyliodide in dichloromethane, carbon tetrachloride or acetonitrile at -78.degree. C. to 50.degree. C.; lithium iodide in pyridine or quinoline at temperatures from 100.degree. to 250.degree. C. and one or more molar equivalents of ethyl, methyl or isopropyl mercaptan in the presence of one or more molar equivalents of a Lewis acid such as aluminum trichloride or boron trifluoride in a solvent such as dichloromethane at temperatures ranging from -78.degree. C. to 50.degree. C. ##STR6##
Further derivatives of the compounds of formula (I) in Scheme 3 can be prepared by the following methods. The compound of formula (Id: R.sup.1 is H) (Scheme 3) can be acylated on the phenolic oxygen using one or more molar equivalents of suitable acylating agent to provide the compounds of formula (Id: R.sup.1 is OCOR; R is lower alkyl). The acylating agent is generally a lower alkyl or aryl carboxylic acid anhydride or a lower alkyl or aryl carboxylic acid chloride. The reaction is run under standard conditions, for example, the use of pyridine as solvent with or without a co-solvent such as dichloromethane at 0.degree. C. to room temperature. The acylated phenols of formula (Id: R.sup.1 is OCOR; R is lower alkyl) can then be brominated in the 2-position of the dibenzothiophene ring to form the acylated bromophenols of formula (Ie: B, D is H; R.sup.1 is OCOR; R is lower alkyl; X is Br) (Scheme 3). This bromination reaction is generally done using 1 to 1.3 molar equivalents of molecular bromine in an inert solvent such as dichloromethane or carbon tetrachloride at temperatures ranging from -78 .degree. C. to room temperature.
Using a similar bromination reaction, the phenols of formula (le: B, D is lower alkyl; R.sup.1, X is H) can then be brominated in the 2-position of the dibenzothiophene ring to form the bromophenols of formula (Ie: B, D is lower alkyl; R.sup.1 is H; X is Br) (Scheme 3). This bromination reaction is generally done using 1 to 1.3 molar equivalents of molecular bromine in an inert solvent such as dichloromethane or carbon tetrachloride at temperatures ranging from -78 .degree. C. to room temperature.
The acyl group can then be removed from the acylated bromophenols of formula (Ie: B, D is H; R.sup.1 is OCOR; R is lower alkyl; X is Br) to provide the bromophenols of formula (Ie: B, D, R.sup.1 is H; X is Br) (Scheme 3) using standard conditions. These conditions include aqueous base in which one or more molar equivalents of alkali metal hydroxide such as sodium hydroxide is used in water with a co-solvent such as THF, dioxane or a lower alcohol such as methanol or mixtures of THF and a lower alcohol at temperatures ranging from 0.degree. C. to 40.degree. C. Acid conditions may also be employed in which the compound is reacted with one or more molar equivalents of a mineral acid such as HCl or sulfuric acid in water with or without a co-solvent such as THF at temperatures ranging from room temperature to 80.degree. C.
The phenols of formula (Ie: B, D, R.sup.1 is H; X is H, Br) can be brominated in two positions to afford the bromophenols of formula (Ie: B, D is Br; R.sup.1 is H; X is H, Br) using at least 2 molar equivalents of molecular bromine in an appropriate solvent such as acetic acid. One to fifty molar equivalents of a salt of acetic acid such as potassium or sodium acetate can also be used as a co-reagent in this reaction although it is not absolutely required. ##STR7##
Further derivatives of the compounds of formula (I) in Scheme 4 can be prepared by the following methods. The phenols of formula (If: B, D, X is H, Br) can be alkylated with one or more molar equivalents of an alkyl haloacetate of formula (X.sup.2 CH.sub.2 CO.sub.2 R.sup.3 where X.sup.2 is Cl, Br or I and R.sup.3 is lower alkyl) and with one or more molar equivalents of an alkali metal carbonate such as potassium carbonate in a polar aprotic solvent such as DMF to afford the alkylated product of formula (Ig: B, D, X is H, Br; W is CO.sub.2 R.sup.3 ; R.sup.2 is H; R.sup.3 is lower alkyl).
The phenols of formula (If: B, D, X is H, Br) can be reacted with a 2-hydroxy carboxylic acid ester of formula CH(OH)(R.sup.2)CO.sub.2 R.sup.3 (R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl); R.sup.3 is lower alkyl) to afford the esters of formula (Ig: B, D, X is H, Br; W is CO.sub.2 R.sup.3 ; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl); R.sup.3 is lower alkyl) under the conditions of the Mitsunobu Reactions (for a review see Oyo Mitsunobu Synthesis. 1981, 1-27). The other co-reagents necessary to effect the Mitsunobu Reaction include one or more molar equivalents of a lower alkyl azodicarboxylate diester such as diethyl azodicarboxylate or diisopropyl azodicarboxylate and one or more molar equivalents of triarylphosphine such as triphenylphosphine in a suitable solvent such as diethyl ether, THF, benzene or toluene at temperatures ranging from -20.degree. C. to 120.degree. C.
The 2-hydroxy carboxylic acid ester of formula CH(OH)(R.sup.2)CO.sub.2 R.sup.3 (R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl); R.sup.3 is lower alkyl) are commercially available or can be prepared from commercially available carboxylic acid precursors under standard esterification conditions. (S)-(+)-2-Hydroxy-1-oxo-3-dihydro-2-isoindolinebutyric acid, methyl ester can be prepared from (S)-(+)-2-hydroxy-1,3-dioxo-2-isoindolinebutyric acid, methyl ester via sequential treatment with 1) sodium borohydride in THF-water; 2) trifluoroacetic acid/chloroform; 3) triethylsilane/trifluoroacetic acid and 4) aqueous sodium bicarbonate. 3-(Pyridin-3-yl)-phenyllactic acid, ethyl ester can be prepared according to the two step procedure of B. A. Lefker, W. A. Hada, P. J. McGarry Tetrahedron Lett. 1994, 35, 5205-5208, from commercially available 3-pyridinecarboxaldehyde and ethyl chloroacetate.
The esters of formula (Ig: B, D, X is H, Br; W is CO.sub.2 R.sup.3 ; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl); R.sup.3 is lower alkyl) can be transformed into their carboxylic acid analogs using standard conditions to afford the carboxylic acids of formula (Ig: B, D, X is H, Br; W is CO.sub.2 H; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl)). The conditions to effect these transformations include aqueous base in which one or more molar equivalents of alkali metal hydroxide such as sodium hydroxide is used in water with a co-solvent such as THF, dioxane or a lower alcohol such as methanol or mixtures of THF and a lower alcohol at temperatures ranging from 0.degree. C. to 40.degree. C. Alternatively, acid conditions may also be employed in which the above mentioned carboxylic acid ester of formula (Ig) is reacted with one or more molar equivalents of a mineral acid such as HCl or sulfuric acid in water with or without a co-solvent such as THF at temperatures ranging from room temperature to 80.degree. C. Still alternatively, many other conditions may be employed to effect the above mentioned ester to acid transformation leading to (Ig). These include reacting the carboxylic acid ester of formula (Ig) with one or more molar equivalents of boron tribromide or boron trichloride in dichloromethane at -78.degree. C. to room temperature; one or more molar equivalents hydrobromic acid in acetic acid at 0.degree. C. to 50.degree. C.; one or more molar equivalents trimethylsilylbromide or trimethylsilyliodide in dichloromethane, carbon tetrachloride or acetonitrile at -78.degree. C. to 50.degree. C.; one or more molar equivalents lithium iodide in pyridine or quinoline at temperatures from 100.degree. to 250.degree. C.
The phenols of formula (If: B, D, X is H, Br) can be alkylated with one or more molar equivalents of diethyl trifluoromethylsulfonyloxymethylphosphanate (D. P. Phillion and S. S. Andrew Tet. Lett. 1986, 1477-1480) and with one or more molar equivalents of an alkali metal hydride such as sodium hydride in a suitable solvent such as THF or DMF to afford the diethylphosphonate product of formula (Ig: B, D, X is H, Br; W is PO.sub.3 Et.sub.2 ; R.sup.2 is H).
The phenols of formula (If: B, D, X is H, Br) can be reacted with a 2-hydroxy phosphonic acid diester of formula CH(OH)(R.sup.2)PO.sub.3 (R.sup.3).sub.2, (R.sup.2 is H, lower alkyl, aralkyl, aryl; R.sup.3 is lower alkyl) to afford the phosphonic acid diesters of formula (Ig: B, D, X is H, Br; W is PO.sub.3 (R.sup.3).sub.2 ; R.sup.2 is H, lower alkyl, aralkyl, aryl; R.sup.3 is lower alkyl) under the conditions of the Mitsunobu Reactions (for a review see Oyo Mitsunobu Synthesis 1981, 1-27). The other co-reagents necessary to effect the Mitsunobu Reaction include one or more molar equivalents of a lower alkyl azodicarboxylate diester such as diethyl azodicarboxylate or diisopropyl azodicarboxylate and one or more molar equivalents of triarylphosphine such as triphenylphosphine in a suitable solvent such as diethyl ether, THF, benzene or toluene at temperatures ranging from -20.degree. C. to 120.degree. C.
The 2-hydroxy phosphonic acid diester of formula CH(OH)(R.sup.2)PO.sub.3 R.sup.3 (R.sup.2 is H, lower alkyl, aralkyl, aryl; R.sup.3 is lower alkyl) can be prepared by reacting a dialklylphosphonate of formula HP(O)(OR.sup.3).sub.2 (R.sup.3 is lower alkyl) with an aldehyde of formula R.sup.2 CHO (R.sup.2 is lower alkyl, aryl, aralkyl) under standard conditions.
The phosphonic acid diesters of formula (Ig: B, D, X is H, Br; W is PO.sub.3 (R.sup.3).sub.2 ; R.sup.2 is H, lower alkyl, aralkyl, aryl; R.sup.3 is lower alkyl) can be transformed into their phosphonic acid analogs using standard conditions to afford the phosphonic acids of formula (Ig: B, D, X is H, Br; W is PO.sub.3 (H).sub.2 ; R.sup.2 is H, lower alkyl, aralkyl, aryl). The conditions that may also be employed in which the above mentioned phosphonic acid diester of formula (Ig) is reacted with two or more molar equivalents of a mineral acid such as HCl or sulfuric acid in water with or without a co-solvent such as THF at temperatures ranging from 40 to 100.degree. C. Still alternatively, many other conditions may be employed to effect the above mentioned diester to acid transformation leading to (Ig). These include reacting the phosphonic acid diester of formula (Ig) with two or more molar equivalents of boron tribromide or boron trichloride in dichloromethane at -78.degree. C. to room temperature; two or more molar equivalents hydrobromic acid in acetic acid at 0.degree. C. to 50.degree. C.; two or more molar equivalents trimethylsilylbromide or trimethylsilyliodide in dichloromethane, carbon tetrachloride or acetonitrile at -78.degree. C. to 50.degree. C.; two or more molar equivalents lithium iodide in pyridine or quinoline at temperatures from 60.degree. to 250.degree. C.
The esters of formula (Ig: B, D, X is H, Br; W is CO.sub.2 R.sup.3 ; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl); R.sup.3 is lower alkyl) can be transformed into their primary carboxylic acid amide analogs of formula (Ig: B, D, X is H, Br; W is CO.sub.2 NH.sub.2 ; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl)) by reacting the ester starting material with ammonia gas dissolved in a lower alcohol solvent such as methanol or ethanol at temperatures ranging from 0.degree. C. to 100.degree. C.
Alternatively, the carboxylic acids of formula (Ig: B, D, X is H, Br; W is CO.sub.2 H; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl)) can be transformed into their carboxylic acid amide analogs of formula (Ig: B, D, X is H, Br; W is CO.sub.2 NH.sub.2 ; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl)). This transformation can be accomplished using standard methods to effect carboxylic acid to carboxylic acid amide transformations. These methods include converting the acid to an activated acid and reacting with one or more molar equivalents of the desired amine. Amines in this category include ammonia in the form of ammonium hydroxide, hydroxyl amine and 2-aminopropionitrile. Methods to activate the carboxylic acid include reacting said acid with one or more molar equivalents of oxalyl chloride or thionyl chloride to afford the carboxylic acid chloride in a suitable solvent such as dichloromethane, chloroform or diethyl ether. This reaction is often catalyzed by adding small amounts (0.01 to 0.1 molar equivalents) of dimethylformamide. Other methods to activate the carboxylic acid include reacting said acid with one or more molar equivalents dicyclohexylearbodiimide with or without one or more molar equivalents of hydroxybenzotriazole in a suitable solvent such as dichloromethane or dimethylformamide at temperatures ranging from 0.degree. C. to 60.degree. C.
The phenols of formula (If: B, D, X is H, Br) can be alkylated with one or more molar equivalents of a haloacetonitrile of formula (X.sup.2 CH.sub.2 CN where X.sup.2 is Cl, Br or I) and with one or more molar equivalents of an alkali metal carbonate such as potassium carbonate in a polar aprotic solvent such as DMF to afford the nitriles of formula (Ig: B, D, X is H, Br; W is CN; R.sup.2 is H).
Alternatively, the carboxylic acid amide analogs of formula (Ig: B, D, X is H, Br; W is CO.sub.2 H; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl)) can be converted to their nitrile analogs of formula (Ig: B, D, X is H, Br; W is CN; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl)) by using reagents that dehydrate the primary carboxamide function to the nitrile function. One set of conditions to effect this transformation include reacting the said primary carboxylic acid amide with one or more molar equivalents of trifluoroacetic anhydride and two or more molar equivalents of pyridine in a suitable solvent such as dioxane at temperatures ranging from 60.degree. C. to 120.degree. C.
The nitrites analogs of formula (Ig: B, D, X is H, Br; W is CN; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl)) can be converted to the tetrazoles of formula (Ig: B, D, X is H, Br; W is 5-tetrazole; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1,3-dioxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), CH.sub.2 (3-pyridyl)) by reacting the nitrile function with one or more molar equivalents of trimethylaluminum and one or more molar equivalents of trimethylsilyl azide in a suitable solvent such as benzene or toluene at temperatures ranging from 60.degree. C. to 120.degree. C. Alternatively, the nitrile function can be reacted with one or more molar equivalents of ammonium azide in a suitable solvent such as dimethylformamide at temperatures ranging from 60.degree. C. to 160.degree. C. ##STR8##
Further derivatives of the compounds of formula (I) in Scheme 5 can be prepared by the following methods. The phenols of formula (Ih: B, D, X is H, Br) can be reacted with one or more molar equivalents of lithium (bis)trimethylsilylamide at temperatures ranging from -78.degree. C. to room temperature and the lithium salt can be further reacted with one or more molar equivalents of 5-bromothiazolidine-2,4-dione (prepared according to the method of Zask, et al., J. Med Chem, 1990, 33, 1418-1423) using a suitable solvent such as THF under an inert atmosphere at temperatures ranging from -78.degree. C. to room temperature to provide the compounds of formula (Ii: R.sup.1 is (R, S)-5-thiazolidine-2,4-dione; B, D, X is H, Br).
Alternatively, the phenols of formula (Ih: B, D, X is H, Br) can be reacted with one or more molar equivalents of tetrazole and di-tert-butyl N,N-diethylphosporamidate in THF at room temperature followed by addition of one or more molar equivalents of meta-chlorobenzoic acid at 40.degree. C. according to the procedure of J. W. Perich and R. B. Johns, Synthesis, 1988, 142-144) to afford the phosphate diesters of formula (Ii: R.sup.1 is P(O)(OtBu).sub.2 ; B, D, X is H, Br). These phosphate diesters are then treated with one or more molar equivalents hydrochloric acid in a suitable solvent such as dioxane to provide the phosphonic acids of formula (Ii: R.sup.1 is P(O)(OH).sub.2 ; B, D, X is H, Br).
The phenols of formula (Ih: B, D, X is H, Br) can be transformed to the carboxylic acids of formula (Ii: R.sup.1 is C(CH.sub.3).sub.2 CO.sub.2 H; B, D, X is H, Br) by treatment of the phenols with two or more molar equivalents of solid sodium hydroxide followed by one or more molar equivalents of 1,1,1-trichloro-2-methyl-2-propanol tetrahydrate in the presence of a large excess of acetone which also serves as solvent.
The phenols of formula (Ih: B, D, X is H, Br) can be transformed to the carboxylic acids of formula (Ii: R.sup.1 is CH.sub.2 CH.sub.2 CO.sub.2 H; B, D, X is H, Br) by treatment with one or more molar equivalents of O-propiolactone and treatment with one or more molar equivalents of potassium tert-butoxide in a suitable solvent such as THF.
The phenols of formula (Ih: B, D, X is H, Br) can be reacted with a 3-hydroxy carboxylic acid ester of formula CH(OH)(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3 (R.sup.4 is H or lower alkyl; R.sup.3 is lower alkyl) to afford the esters of formula (Ii: R.sup.1 is CH(OH)(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3 ; R.sup.4 is H or lower alkyl; R.sup.3 is lower alkyl; B, D, X is H, Br) under the conditions of the Mitsunobu Reactions (for a review see Oyo Mitsunobu Synthesis 1981, 1-27). The other co-reagents necessary to effect the Mitsunobu Reaction include one or more molar equivalents of a lower alkyl azodicarboxylate diester such as diethyl azodicarboxylate or diisopropyl azodicarboxylate and one or more molar equivalents of triarylphosphine such as triphenylphosphine in a suitable solvent such as diethyl ether, THF, benzene or toluene at temperatures ranging from -20.degree. C. to 120.degree. C. at temperatures ranging from -20.degree. C. to 120.degree. C.
The 3-hydroxy carboxylic acid ester of formula CH(OH)(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3 (R.sup.4 is H or lower alkyl; R.sup.3 is lower alkyl) are commercially available or can be prepared from commercially available carboxylic acid precursors under standard esterification conditions.
The esters of formula (Ii: R.sup.1 is CH(OH)(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3 ; R.sup.4 is H or lower alkyl; R.sup.3 is lower alkyl; B, D, X is H, Br) can be transformed to the acids of formula (Ii: R.sup.1 is CH(OH)(R.sup.4)CH.sub.2 CO.sub.2 H; R.sup.4 is H or lower alkyl; B, D, X is H, Br) by several standard conditions which include reacting the ester of formula (Ii) with two or more molar equivalents of a mineral acid such as HCl or sulfuric acid in one or more solvents or a combination of two or more solvents such as water, THF or dioxane at temperatures ranging from 40 to 1 20.degree. C. Still alternatively, many other conditions may be employed to effect the above mentioned ester to acid transformation. These include reacting the esters of formula (Ii) with two or more molar equivalents of boron tribromide or boron trichloride in dichloromethane at -78.degree. C. to room temperature; two or more molar equivalents hydrobromic acid in acetic acid at 0.degree. C. to 50.degree. C.; two or more molar equivalents trimethylsilylbromide or trimethylsilyliodide in dichloromethane, carbon tetrachloride or acetonitrile at -78.degree. C. to 50.degree. C.; two or more molar equivalents lithium iodide in pyridine or quinoline at temperatures from 60.degree. to 250.degree. C. ##STR9##
Further derivatives of the compounds of formula (I) in Scheme 6 can be prepared by the following methods. The compounds of formula (Ij: B, D is H, halogen, CN, lower alkyl, aryl, aralkyl; X is H, halogen; R.sup.1 is H, lower alkyl, (R)-CH(R.sup.2)W, (S)-CH(R.sup.2)W, (R, S)-CH(R.sup.2)W, C(CH.sub.3).sub.2 CO.sub.2 R.sup.3, (R,S)-5-thiazolidine-2,4-dione, (R)-CH(R.sup.7)CH.sub.2 CO.sub.2 R.sup.3, (S)-CH(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3, COR.sup.3, PO.sub.3 (R.sup.3).sub.2 ; R.sup.2 -aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), W is CO.sub.2 R.sup.3, CONH.sub.2, CN, 5-tetrazole, PO.sub.3 (R.sup.3).sub.2 ; R.sup.3 is H or low aryl; R.sup.4 is H or lower alkyl) can be transformed into their sulfoxide derivatives of formula (Ik: n is 1; B, D is H, halogen, CN, lower alkyl, aryl, aralkyl; X is H, halogen; R.sup.1 is H, lower alkyl, (R)-CH(R.sup.2)W, (S)-CH(R.sup.2)W, (R, S)-CH(R.sup.2)W, C(CH.sub.3).sub.2 CO.sub.2 R.sup.3, (R,S)-5-thiazolidine-2,4-dione, (R)-CH(R.sup.7)CH.sub.2 CO.sub.2 R.sup.3, (S)-CH(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3, COR.sup.3, PO.sub.3 (R.sup.3).sub.2 ; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), W is CO.sub.2 R.sup.3, CONH.sub.2, CN, 5-tetrazole, PO.sub.3 (R.sup.3).sub.2 ; R.sup.3 is H or lower alkyl, aryl; R.sup.4 is H or lower alkyl) using one molar equivalent of an oxidizing agent such as m-chloroperbenzoic acid in dichloromethane at temperatures ranging from -20.degree. C. to 40.degree. C. or peracetic acid in acetic acid and water at temperatures ranging from room temperature to 100.degree. C.
The compounds of formula (Ij: B, D is H, halogen, CN, lower alkyl, aryl, aralkyl; X is H, halogen; R.sup.1 is H, lower alkyl, (R)-CH(R.sup.2)W, (S)-CH(R.sup.2)W, (R, S)-CH(R.sup.2)W, C(CH.sub.3).sub.2 CO.sub.2 R.sup.3, (R,S)-5-thiazolidine-2,4-dione, (R)-CH(R.sup.7)CH.sub.2 CO.sub.2 R.sup.3, (S)-CH(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3, COR.sup.3, PO.sub.3 (R.sup.3).sub.2 ; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), W is CO.sub.2 R.sup.3, CONH.sub.2, CN, 5-tetrazole, PO.sub.3 (R.sup.3).sub.2 ; R.sup.3 is H or lower alkyl, aryl; R.sup.4 is H or lower alkyl) can be transformed into their sulfone derivatives of formula (1k: n is 2; B, D is H, halogen, CN, lower alkyl, aryl, aralkyl; X is H, halogen; R.sup.1 is H, lower alkyl, (R)-CH(R.sup.2)W, (S)-CH(R.sup.2)W, (R, S)-CH(R.sup.2)W, C(CH.sub.3).sub.2 CO.sub.2 R.sup.3, (R,S)-5-thiazolidine-2,4-dione, (R)-CH(R.sup.7)CH.sub.2 CO.sub.2 R.sup.3, (S)-CH(R.sup.4)CH.sub.2 CO.sub.2 R.sup.3, COR.sup.3, PO.sub.3 (R.sup.3).sub.2 ; R.sup.2 is H, lower alkyl, aralkyl, aryl, CH.sub.2 (1H-imidazol-4-yl), CH.sub.2 (3-1H-indolyl), CH.sub.2 CH.sub.2 (1-oxo-1,3-dihydro-isoindol-2-yl), W is CO.sub.2 R.sup.3, CONH.sub.2, CN, 5-tetrazole, PO.sub.3 (R.sup.3).sub.2 ; R.sup.3 is H or lower alkyl, aryl; R.sup.4 is H or lower alkyl) using two or more molar equivalents of an oxidizing agent such as m-chloroperbenzoic acid in dichloromethane at temperatures ranging from -20.degree. C. to 60.degree. C. or peracetic acid in acetic acid and water at temperatures ranging from room temperature to 100.degree. C.
The compounds of this invention are useful in treating metabolic disorders related to insulin resistance or hyperglycemia, typically associated with obesity or glucose intolerance. The compounds of this invention are therefore, particularly useful in the treatment or inhibition of type II diabetes. The compounds of this invention are also useful in modulating glucose levels in disorders such as type I diabetes.
The ability of compounds of this invention to treat or inhibit disorders related to insulin resistance or hyperglycemia was established with representative compounds of this invention in the following two standard pharmacological test procedures which measure the inhibition of PTPase.
Inhibition of Tri-Phosphorylated Insulin Receptor Dodecaphosphopeptide Dephosphorylation by Rat Hepatic Protein-Tyrosine Phosphatases (PTPases)
This standard pharmacological test procedure assess the inhibition of rat hepatic microsomal PTPase activity using, as substrate, the phosphotyrosyl dodecapeptide corresponding to the 1142-1153 insulin receptor kinase domain, phosphorylated on the 1146, 1150 and 1151 tyrosine residues. The procedure used and results obtained are briefly outlined below.
Preparation of Microsomal Fraction: Rats (Male Sprague-Dawley rats (Charles River, Kingston, N.Y.) weighing 100-150 g, maintained on standard rodent chow (Purina)) are sacrificed by asphyxiation with CO2 and bilateral thoracotomy. The liver is removed and washed in cold 0.85% (w/v) saline and weighed. The tissue is homogenized on ice in 10 volumes of Buffer A and the microsomes are isolated essentially as described by Meyerovitch J, Rothenberg P, Shechter Y, Bonner-Weir S, Kahn C R. Vanadate normalizes hyperglycemia in two mouse models of non-insulin-dependent diabetes mellitus. J Clin Invest 1991; 87:1286-1294 and Alberts B, Bray D, Lewis J, Raff M, Roberts K, Watson J D, editors. Molecular biology of the cell. New York: Garland Publishing, Inc., 1989 with minor modifications. The liver homogenate is filtered through silk to remove any remaining tissue debris and then is centrifuged at 100,000.times.g for 20 minutes at 40.degree. C. The supernatant is decanted and centrifuged at 100,000.times.g for 60 minutes at 40.degree. C. The pellet, microsomes and small vesicles, is resuspended and lightly homogenized in : 20 mM TRIS-HCl (pH 7.4), 50 mM 2-mercaptoethanol, 250 mM sucrose, 2 mM EDTA, 10 mM EGTA, 2 mM AEBSF, 0.1 mM TLCK, 0.1 mM TPCK, 0.5 mM benzamidine, 25 ug/ml leupeptin, 5 ug/ml pepstatin A, 5 ug/ml;H5B antipain, 5 ug/ml chymostatin, 10 ug/ml aprotinin (Buffer A), to a final concentration of approximately 850 ug protein/ml. Protein concentration is determined by the Pierce Coomassie Plus Protein Assay using crystalline bovine serum albumin as a standard (Pierce Chemical Co., Rockford, Ill.).
Measurement of PTPase activity: The malachite green-ammonium molybdate method, as described by Lanzetta P A, Alvarez L J, Reinach P S, Candia O A was used. An improved assay for nanomolar amounts of inorganic phosphate. Anal. Biochem. 1979;100:95-97, and adapted for the platereader, is used for the nanomolar detection of liberated phosphate by rat hepatic microsomal PTPases. The test procedure uses, as substrate, a dodecaphosphopeptide custom synthesized by AnaSpec, Inc. (San Jose, Calif.). The peptide, TRDIYETDYYRK, corresponding to the 1142-1153 catalytic domain of the insulin receptor, is tyrosine phosphorylated on the 1146, 1150 and 1151 tyrosine residues. The microsomal fraction (83.25 ul) is preincubated for 10 min at 37 deg.C. with or without test compound (6.25 ul) and 305.5 ul of the 81.83 mM HEPES reaction buffer, pH 7.4. Peptide substrate, 10.5 ul at a final concentration of 50 uM, is equilibrated to 37 deg.C. in a LABLINE Multi-Blok heater equipped with a titerplate adapter. The preincubated microsomal preparation (39.5 ul) with or without drug is added to initiate the dephosphorylation reaction, which proceeds at 37 deg.C. for 30 ml. The reaction is terminated by the addition of 200 ul of the malachite green-ammonium molybdate-Tween 20 stopping reagent (MG/AM/Tw). The stopping reagent consists of 3 parts 0.45% malachite green hydrochloride, 1 part 4.2% ammonium molybdate tetrahydrate in 4 N HCl and 0.5% Tween 20. Sample blanks are prepared by the addition of 200 ul MG/AM/Tw to substrate and followed by 39.5 ul of the preincubated membrane with or without drug. The color is allowed to develop at room temperature for 30 min and the sample absorbances are determined at 650 nm using a platereader (Molecular Devices). Samples and blanks are prepared in quadruplicates. Screening activity of 50 uM (final) drug is accessed for inhibition of microsomal PTPases.
Calculations: PTPase activities, based on a potassium phosphate standard curve, are expressed as nmoles of phosphate released/min/mg protein. Test compound PTPase inhibition is calculated as percent of control. A four parameter non-linear logistic regression of PTPase activities using SAS release 6.08, PROC NLIN, is used for determining IC50 values of test compounds. All compounds were administered at a concentration of 50 .mu.M. The following results were obtained using representative compounds of this invention.
______________________________________ % Change from Example Control______________________________________ 3 -51.63 6 -31.13 7 -18.53 10 -21.11 12 -19.49 13 -42.62 14 -74.88 19 -81.43 20 -75.69 21 -87.44 Phenylarsine oxide -57.06 (reference standard)______________________________________
Inhibition of Tri-Phosphorylated Insulin Receptor Dodecaphosphopeptide Dephosphorylation by hPTP1B
This standard pharmacological test procedure assess the inhibition of recombinant rat protein tryosine phosphatase, PTP1B, activity using, as substrate, the phosphotyrosyl dodecapeptide corresponding to the 1142-1153 insulin receptor kinase domain, phosphorylated on the 1146, 1150 and 1151 tyrosine residues. The procedure used and results obtained are briefly described below.
Human recombinant PTP1B was prepared as described by Goldstein (see Goldstein et al. Mol. Cell. Biochem. 109, 107, 1992). The enzyme preparation used was in microtubes containing 500-700 .mu.g/ml protein in 33 mM Tris-HCl, 2 mM EDTA, 10% glycerol and 10 mM 2-mercaptoethanol.
Measurement of PTPase activity. The malachite green-ammonium molybdate method, as described (Lanzetta et al. Anal. Biochem. 100, 95, 1979) and adapted for a platereader, is used for the nanomolar detection of liberated phosphate by recombinant PTP1B. The test procedure uses, as substrate, a dodecaphosphopeptide custom synthesized by AnaSpec, Inc. (San Jose, Calif.). the peptide, TRDIYETDYYRK, corresponding to the 1142-1153 catalytic domain of the insulin receptor, is tyrosine phosphorylated on the 1146, 1150, and 1151 tyrosine residues. The recombinant rPTP1B is diluted with buffer (pH 7.4, containing 33 mM Tris-HCl, 2 mM EDTA and 50 mM b-mercaptoethanol) to obtain an approximate activity of 1000-2000 nmoles/min/mg protein. The diluted enzyme (83.25 mL) is preincubated for 10 min at 37.degree. C. with or without test compound (6.25 mL) and 305.5 mL of the 81.83 mM HEPES reaction buffer, pH 7.4 peptide substrate, 10.5 ml at a final concentration of 50 mM, and is equilibrated to 37.degree. C. in a LABLINE Multi-Blok heater equipped with a titerplate adapter. The preincubated recombinant enzyme preparation (39.5 ml) with or without drug is added to initiate the dephosphorylation reaction, which proceeds at 37.degree. C. for 30 min. The reaction is terminated by the addition of 200 mL of the malachite green-ammonium molybdate-Tween 20 stopping reagent (MG/AM/Tw). The stopping reagent consists of 3 parts 0.45% malachite green hydrochloride, 1 part 4.2% ammonium molybdate tetrahydrate in 4 N HCl and 0.5% Tween 20. Sample blanks are prepared by the addition of 200 mL MG/AM/Tw to substrate and followed by 39.5 ml of the preincubated recombinant enzyme with or without drug. The color is allowed to develop at room temperature for 30 min. and the sample absorbances are determined at 650 nm using a platereader (Molecular Devices). Sample and blanks are prepared in quadruplicates.
Calculations: PTPase activities, based on a potassium phosphate standard curve, are expressed as nmoles of phosphate released/min/mg protein. Inhibition of recombinant PTP1B by test compounds is calculated as percent of phosphatase control. A four parameter non-linear logistic regression of PTPase activities using SAS release 6.08, PROC NLIN, is used for determining IC.sub.50 values of test compounds. The following results were obtained.
______________________________________Example IC50 (.mu.M)______________________________________ 7 1.89 19 1.33 20 0.604 21 1.39 Phenylarsine oxide 39.7 (reference standard) Sodium orthovanadate 244.8 (reference standard) Ammonium molybdate 8.7 tetrahydrate (reference standard)______________________________________
Based on the results obtained in the standard pharmacological test procedures, the compounds of this invention have been shown to inhibit PTPase activity, and are therefore useful in treating metabolic disorders related to insulin resistance or hyperglycemia, typically associated with obesity or glucose intolerance. More particularly, the compounds of this invention useful in the treatment or inhibition of type II diabetes, and in modulating glucose levels in disorders such as type I diabetes. As used herein, the term modulating means maintaining glucose levels within clinically normal ranges.
Effective administration of these compounds may be given at a daily dosage of from about 1 mg/kg to about 250 mg/kg, and may given in a single dose or in two or more divided doses. Such doses may be administered in any manner useful in directing the active compounds herein to the recipient's bloodstream, including orally, via implants, parenterally (including intravenous, intraperitoneal and subcutaneous injections), rectally, vaginally, and transdermally. For the purposes of this disclosure, transdermal administrations are understood to include all administrations across the surface of the body and the inner linings of bodily passages including epithelial and mucosal tissues. Such administrations may be carried out using the present compounds, or pharmaceutically acceptable salts thereof, in lotions, creams, foams, patches, suspensions, solutions, and suppositories (rectal and vaginal).
Oral formulations containing the active compounds of this invention may comprise any conventionally used oral forms, including tablets, capsules, buccal forms, troches, lozenges and oral liquids, suspensions or solutions. Capsules may contain mixtures of the active compound(s) with inert fillers and/or diluents such as the pharmaceutically acceptable starches (e.g. corn, potato or tapioca starch), sugars, artificial sweetening agents, powdered celluloses, such as crystalline and microcrystalline celluloses, flours, gelatins, gums, etc. Useful tablet formulations may be made by conventional compression, wet granulation or dry granulation methods and utilize pharmaceutically acceptable diluents, binding agents, lubricants, disintegrants, suspending or stabilizing agents, including, but not limited to, magnesium stearate, stearic acid, talc, sodium lauryl sulfate, microcrystalline cellulose, carboxymethylcellulose calcium, polyvinylpyrrolidone, gelatin, alginic acid, acacia gum, xanthan gum, sodium citrate, complex silicates, calcium carbonate, glycine, dextrin, sucrose, sorbitol, dicalcium phosphate, calcium sulfate, lactose, kaolin, mannitol, sodium chloride, talc, dry starches and powdered sugar. Oral formulations herein may utilize standard delay or time release formulations to alter the absorption of the active compound(s). Suppository formulations may be made from traditional materials, including cocoa butter, with or without the addition of waxes to alter the suppository's melting point, and glycerin. Water soluble suppository bases, such as polyethylene glycols of various molecular weights, may also be used.
It is understood that the dosage, regimen and mode of administration of these compounds will vary according to the malady and the individual being treated and will be subject to the judgement of the medical practitioner involved. It is preferred that the administration of one or more of the compounds herein begin at a low dose and be increased until the desired effects are achieved.

The following procedures describe the preparation of representative examples of this invention.
EXAMPLE 1
2-All-3-yl-benzo[b]thiophene
n-Butyl lithium (16.7 ml, 2.5 N in hexanes) was added dropwise to a stirred solution of thianaphthene (5.0 g, 37.3 mmol) in THF (80 mL) at -78.degree. C. under a dry N2 atmosphere. After the addition wascompleted, the mixture was warmed up and stirred at 0.degree. C. for 30 min. Allylbromide (16.1 mL, 186.5 mmol ) was added. After an additional 3.5 h., sat. aq. NH4Cl was added and the reaction mixture was partitioned between water and ether. The ether phase was washed with brine and dried. Silica gel (120 mL) was added. Solvents were removed and the silica adsorbate was flash chromatographed (eluent petroleum ether) to provide the title compound as an oil (3.74 g, 58%): NMR (CDCl3); .delta. 7.76 (d, J=9 Hz, 1H), 7.66 (d, J=9 Hz, 1H), 7.36-7.20 (m, 2H), 7.02 (s, 1H), 6.14-5.96 (m, 1H), 5.22 (dd, J=2, 17 Hz, 1H), 5.16 (dd, J=2, 17 Hz, 1H), 3.66 (d, J=8 Hz, 2H); MS (EI): [M+] 174 (100%); Anal. Calc. for C11H10S: C, 75.82, H, 5.78, N, 0.00. Found: C, 72.88, H, 5.56, N, 0.13.
EXAMPLE 2
(2-All-3-yl-benzo[b]thiophen-3-yl)-(4-methoxy-phenyl)-methanone
Tin tetrachloride (2.83 mL, 24.12 mmol) was added dropwise over a 10 minute period to a stirred solution of 2-all-3-yl-benzo[b]thiophene (3.51 g, 20.1 mmol), anisoyl chloride (3.61 g, 21.1 mmol) and dichloromethane (70 mL) under a dry nitrogen atmosphere. After 5 h., the mixture was warmed up and stirred at 0.degree. C. for 1 h. The reaction mixture was added to water and extracted with ethyl ether. The ethyl ether extract was washed with sat. aq. sodium bicarbonate and brine. Silica gel (100 mL) was added. Solvents were removed and the silica adsorbate was flash chromatographed (eluent 92:8 petroleum ether:ethyl acetate) to provide the title compound as an oil (4.42 g, 71 %): NMR (CDCl3); .delta. 7.88-7.76 (multiplet with overlapping doublet at 7.84, J=9 Hz, 3H), 7.50-7.44 (m, 1H), 7.34-7.24 (m, 2H), 6.94 (d, J=9 Hz, 2H), 6.00-5.85 (m, 1H), 5.20-5.13 (m, 2H), 3.90 (s, 3H), 3.62 (d, J=6 Hz, 2H); MS (EI): [M+] 308 (50%); Anal. Calc. for C19H16O2S: C, 74.00, H, 5.23, N, 0.00. Found: C, 73.16, H, 5.13, N, 0.09.
EXAMPLE 3
4-(Dibenzothiophen-1-yl)-phenol
To a mechanically stirred, cold (-74.degree. C. dry ice-isopropanol bath) solution of (2-allyl-benzothiophen-3-yl)-(4-methoxy-phenyl)-methanone (11.27 g, 36.5 mmol) in anhydrous methylene chloride (112 mL) was added a 1 M solution of boron tribromide in methylene chloride (146 mL, 146 mmol, 4 eq) dropwise over a period of 1.25 hours under a dry nitrogen atmosphere. The reaction mixture was stirred in the warming bath overnight and at ambient temperature for 6 days. The reaction mixture was diluted with methylene chloride (total volume 500 mL) and added cautiously to water (1 L) with cooling in an ice bath. The layers were separated and the aqueous phase was extracted with ether (500 mL). The organic phases were combined, washed with a dilute aqueous solution of sodium bisulfite (2.times.1 L), and combined with silica gel. The solvents were removed and the adsorbate was flash chromatographed (82/18 petroleum ether/ethyl acetate) and chased with benzene and petroleum ether to provide the title compound as a white solid (5.79 g, 57%): mp 117-119.degree. C.; NMR (CDCl3): .delta. 7.84 (dd, J=8, 1 Hz, 1H), 7.82 (dm, J=8 Hz, 1H), 7.45 (dd, J=8, 8, 1 Hz, 1H), 7.37-7.31 (multiplet with overlapping doublet at 7.33, J=8 Hz, 3H), 7.25 (s, 1H), 7.24 (dd, J=7, 1 Hz, 1H), 7.22 (dm, J=7 Hz, 1H), 7.10 (ddd, J=8, 7, 1 Hz, 1H), 7.01-6.98 (multiplet with overlapping doublet at 6.98, J=8 Hz, 2H); MS (EI): [M+] 276 (100%); Anal. Calc. for C18H12OS: C, 78.23, H, 4.38, N, 0.00. Found: C, 77.83, H, 4.22, N, 0.05.
EXAMPLE 4
Acetic acid 4-dibenzothiophen-1-yl)-phenyl ester
Acetic anhydride (0.62 mL, 6.55 mmol) was added to a stirred 0.degree. C., solution of 4-(6-bromo-dibenzothiophen-1-yl)-phenol (1.69 g, 6.12 mmol) in pyridine (8 mL). After 5.5 h the reaction mixture was added to water and the resulting oil mixture was extracted with methylene chloride. The combined methylene chloride extracts were washed with water, dried with brine and anhydrous MgSO4, and then concentrated in vacuo to provide the title compound as an off-white solid (1.88 g, 96.4%): MS (EI): [M+H]+ 319.
EXAMPLE 5
4-[2-Bromo-(dibenzothiophen-1-yl)]1-phenol acetate ester
A solution of bromine (0.359 mL, 6.97 mmol) in dichloromethane (11 mL) was added dropwise over a 30 min. period to a stirred, -20.degree. C. solution of Acetic acid 4-dibenzothiophen-1-yl)-phenyl ester (2.22 g, 6.03 mmol) in dichloromethane (37 mL). This solution was stirred for 24 h., and then quenched with 10% aqueous sodium bisulfide and further diluted with water (100 mL). The aqueous mixture was extracted with ethyl ether. The ethyl ether extracts were washed with water, dried with brine and anhydrous MgSO4, and concentrated to provide a semi-solid. The solid was purified by HPLC (C18 Column, 75:25 acetonitrile:water) to provide the title compound as a solid (0.955 g, 41%): mp 114.5-116.degree. C.; NMR (CDCl3); .delta. 7.80 (ddd, J=8,1,1 Hz, 1H), 7.74 (s, 2H), 7.38-7.32 (m, 5H), 7.08 (t, J=8 Hz, 1H), 6.65 (d, J=8 Hz, 1H), 2.38 s, 3H); MS[EI]: [M+*]@ m/z 396(45%), 398(50%), 354(65%), 356(100%); Anal. Calc. for C20H13BrO2S: C, 60.46, H, 3.30, N, 0.00. Found: C, 60.62, H, 3.06, N, 0.21.
EXAMPLE 6
4-(2-Bromo-dibenzothiophen-1-yl)-phenol
To a solution of 4-[2-bromo-(dibenzothiophen-1-yl)]-phenol acetate ester (0.740 g, 1.86 mmol) in tetrahydrofuran (15 mL) and methanol (5 mL) was added an aqueous solution of potassium hydroxide (1 N, 2.79 mL, 2.79 mmol, 1.5 eq) dropwise at room temperature. After stirring 1.5 hours the solvents were removed and water (60 mL) was added to the residue. The mixture was acidified with 10% hydrochloric acid and the white solid was filtered to give the title compound (0.540 g, 82%); mp 185-186.degree. C.; MS [EI] M*+ m/z 354(90%), 356(100%), 1 bromine isotope pattern observed, Anal. Calc. for C18H11BrOS: C, 60.86, H, 3.12, N, 0.00, Found: C, 61.04, H, 2.94, N, 0.09.
EXAMPLE 7
2,6-Dibromo-4-(dibenzothiophen-1-yl)-phenol
A solution of 4-(dibenzothiophen-1-yl)-phenol (1.00 g, 3.62 mmol) and potassium acetate (3.55 g, 36.2 mmol, 10 eq) in glacial acetic acid (30 mL) was cooled in an ice bath until solid just starts to form. A solution of bromine (0.41 mL, 7.96 mmol, 2.2 eq) in glacial acetic acid (10 mL) was added dropwise over a period of 20 minutes. After stirring for 0.5 hours water (100 mL) was added followed by the addition of dilute sodium thiosulfite (500 mL). The resulting solid was collected on a sintered glass funnel. Recrystallization from boiling acetic acid (14 mL) with hot filtration provided the title compound as a white solid (1.106 g, 70%): mp 128-130.degree. C.; NMR (DMSO-d6): .delta. 10.24 (broad s, 1H), 8.07 (ddd, J=8, 2, 1 Hz, 1H), 8.03 (dm, J=8 Hz, 1H), 7.63 (s, 2H), 7.53 (ddd, J=8, 8, 1 Hz, 1H), 7.43 (ddd, J=8, 8, 1 Hz, 1H), 7.28 (dm, J=7 Hz, 1H), 7.24 (dm, J=7 Hz, 1H), 7.16 (d, J=8 Hz, 1H); MS (+FAB): [M+], 2 bromine isotope pattern, 432 (50%), 434 (100%), 436 (49%); Anal. Calc. for C18H10Br2OS: C, 49.80, H, 2.32, N, 0.00. Found: C, 49.41, H, 2.04, N, 0.05.
EXAMPLE 8
2,6-Dibromo-4-(6-bromo-dibenzothiophen-1-yl)-phenol
A solution of bromine (0.452 mL, 8.8 mmol) in glacial acetic acid (12 mL) was added over a twenty-five minute period to a stirred solution of 4-(6-bromo-dibenzothiophen-1-yl)-phenol (0.709 g, 2.0 mmol), potassium acetate (1.96 g, 20.0 mmol) in acetic acid (28 mL) at ambient temperature. After 3 h., the reaction mixture was quenched with 10% aqueous sodium bisulfide and further diluted with water (100 mL). Aqueous mixture was extracted with dichloromethane (120 mL). The dichloromethane extract was washed with water, dried with brine and anhydrous MgSO4, and concentrated to provide the title compound as an off-white solid (1.27 g, 100%): NMR (CDCl3); .delta. 7.83 (d, J=8 Hz, 1H), 7.74 (d, J=1 Hz, 2H), 7.46 (s, 2 H), 7.44 (ddd, J=8, 1, 1 Hz, 1H), 7.18 (ddd, J=8, 7, 1 Hz, 1H), 6.88 (d, J=8 Hz, 1H), 6.13 (s, 1H, OH); mp 118-119.degree. C.: MS (EI): [M+], 3 bromine isotope pattern, 510, 512, 514, 516.
EXAMPLE 9
[4-(Dibenzothiophen-1-yl)-phenoxy]-acetic acid methyl ester
To a solution of 4-(dibenzothiophen-1-yl)-phenol (1.00 g, 3.62 mmol) and potassium carbonate (0.676 g, 4.89 mmol, 1.35 eq) in N,N-dimethylformamide (5 mL) was added methylbromoacetatc (0.685 mL, 7.24 mmol, 2 eq) dropwise at room temperature under a dry nitrogen atmosphere. After stirring 17 hours at room temperature the reaction mixture was poured into water (80 mL) and the solid precipitate was filtered. The solid was dissolved in methylene chloride and combined with silica gel. The adsorbate was flash chromatographed (40/60 petroleum ether/methylene chloride) to provide the title compound as a white solid (1.08 g, 85%): mp 148-149.5.degree. C.; NMR (CDCl3): .delta.0 7.85 (dd, J=8, 1 Hz, 1H), 7.81 (d, J=8 Hz, 1H), 7.45 (dd, J=8, 7 Hz, 1H), 7.46-7.43 (m, 2H), 7.41-7.37 (m, 1H), 7.34 (ddd, J=8, 7, 1 Hz, 1H), 7.24 (dd, J=7, 1 Hz, 1H), 7.18 (ddd, J=8, 7, 1 Hz, 1H), 7.12-7.04 (m, 2H), 4.76 (s, 2H), 3.87 (s, 3H); MS (EI): [M+] 348; High Resolution MS: Calc. Sample mass 348.082018 for formula C21H16O3S, measured mass 348.08451, mass deviation 2.5 memu. Anal. Calc. for C21H16O3S: C, 72.39, H, 4.63, N, 0.00. Found: C, 70.84, H, 4.42, N, 0.06. 98% Pure by Analytical HPLC.
EXAMPLE 10
[4-(2-Bromo-dibenzothiophen-1-yl)-phenoxy]-acetic Acid Methyl Ester
To a solution of 4-(2-bromo-dibenzothiophen-1-yl)-phenol (0.480 g, 1.35 mmol) and potassium carbonate (0.385 g, 2.79 mmol, 2.06 eq) in anhydrous N,N-dimethylformamide (3 mL) was added methylbromoacetate (0.255 mL, 2.07 mmol, 2 eq) dropwise at room temperature under a dry nitrogen atmosphere. After stirring 24 hours the reaction mixture was poured into water (100 mL) and the organics were extracted into ether (100 mL) The ether was washed with water (100 mL) and brine (100 mL). Silica gel was added and the solvents removed. The adsorbate was flash chromatographed (55/45 petroleum ether/methylene chloride) and dried in vacuo at 58.degree. C. to provide the title compound as a white solid (0.509 g, 88%); mp 122-122.5.degree. C. NMR (DMSO-d6), .delta. 8.02 (d, J=8 Hz, 1H), 8.00 (d, J=8 Hz, 1H), 7.83 (d, J=8 Hz, 1H), 7.41 (t, J=8 Hz, 1H), 7.26-7.20 (m, 2H), 7.19 -7.16 (m, 2H), 7.13-7.09 (ddd, J=8,7,1, 1H), 6.53 (d, J=8 Hz 1H), 4.94 (s, 2H), 3.75 (s, 3H), MS [PBEI] M*+ m/z=426(100%), 428(98%), 1 bromine isotope pattern detected, Anal. Calc. for C21H15O3SBr: C, 59.03, H, 3.54, N, 0.00. Found: C, 58.91, H, 3,27, N, -0.02.
EXAMPLE 11
[2,6-Dibromo-4-(dibenzothiophen-1-yl)-phenoxy]-acetic acid, ethyl ester
To a solution of 2,6-dibromo-4-dibenzothiophen-1-yl)-phenol (0.100 g, 0.230 mmol) and rhodium (II) acetate dimer (0.010 g, 0.1 mole percent) in dry benzene (5 mL) was added ethyl diazoacetate (0.036 mL, 0.345 mmol, 1.5 eq) dropwise at room temperature under a dry nitrogen atmosphere. After heating to reflux for 5 hours and standing at ambient temperature for 19 hours additional rhodium (II) acetate dimer (0.010 g, 0.1 mole percent) and ethyl diazoacetate (0.072 mL, 0.690 mmol, 3 eq) were added. The reaction mixture was heated to reflux for 20.5 hours. The solvent was removed and the residue was flash chromatographed (70/30 petroleum ether/methylene chloride) to provide the title compound as a white solid (0.052 g, 43%); mp 140.5-142.degree. C.; NMR (CDCl3): .delta. 7.90 (dd, J=8, 1 Hz, 1H), 7.85 (d, J=8 Hz, 1H), 7.65 (s, 2H), 7.47 (t, J=8 Hz, 1H), 7.40 (ddd, J=8, 6, 2 Hz, 1H), 7.24-7.12 (m, 3H), 4.77 (s, 2H), 4.38 (q, J=7 Hz, 2H), 1.39 (t, J=7 Hz, 3 H); MS (EI): [M+], 2 bromine isotope pattern, 518 (44%), 520 (100%), 522 (48%); Anal. Calc for C22H16Br2O3S: C, 50.79, H, 3.10, N, 0.00. Found: C, 51.15, H, 3.08, N, 0.12.
EXAMPLE 12
[4-(Dibenzothiophen-1-yl)-phenoxy]-acetic Acid
To a solution of [4-(dibenzothiophen-1-yl)-phenoxy]-acetic acid methyl ester (0.911 g, 2.61 mmol) in tetrahydrofuran (15 mL) and methanol (5 mL) was added an aqueous solution of potassium hydroxide (1N, 3.10 mL, 3.10 mmol, 1.2 eq) dropwise at room temperature. After stirring 1 hour at room temperature the solvents were removed. The residue was dissolved in water (125 mL) and was acidified with 10% aqueous hydrochloric acid. The water was removed and the solid was triturated in petroleum ether. Recrystallization from boiling acetic acid with hot filtration to give the title compound as a white crystalline solid (0.458 g, 52%): mp 169.5-170.5.degree. C.; NMR (CDCl3): .delta. 7.88-7.81 (m, 2H), 7.48-7.39 (m, 3H), 7.37-7.32 (m, 1H), 7.26-7.17 (m, 2H), 7.13-7.08 (m, 3H), 4.83 (s, 2H); MS (El): [M+] 334; Anal. Calc. for C20H14O3S: C, 71.84, H, 4.22, N, 0.00. Found: C, 71.04, H, 3.90, N, 0.09.
EXAMPLE 13
[4-(2-Bromo-dibenzothiophen-1-yl)-phenoxy]-acetic Acid
To a solution of [4-(2-bromo-dibenzothiophen-1-yl)-phenoxy]-acetic acid methyl ester (0.449 g, 1.05 mmol) in tetrahydrofuran (15 mL) and methanol (5 mL) was added an aqueous solution of potassium hydroxide (1N, 1.26 mL, 1.2 eq) dropwise at room temperature. After stirring 1 hour at room temperature the solvents were removed and the residue was disolved in water (50 mL) and the reaction mixture was acidified with 10% hydrochloric acid. After stirring 15 minutes the white solid was collected on a sintered glass funnel, washed with water and dried in vacuo at 58.degree. C. overnight to give the title compound as a white solid (0.405 g, 93%); mp 209.5-210.5.degree. C.; NMR (DMSO, d6): .delta. 13.06 (broad singlet), 8.02 (d, J=8 Hz, 1H), 8.01 (dd, J=8,1 Hz, 1H), 7.82 (d, J=8 Hz, 1H), 7.40 (ddd, J=8,7,1 Hz, 1H), 7.26-7.20 (m, 2H), 7.18=7.07 (m, 3H), 6.54 (d, J=8 Hz, 1H), 4.81 (s, 2H); MS [EI] M*+ m/z=412(98%), 414(100%), 1bromine isotope pattern detected, Anal. Calc. for C20H13BrO3S: C, 58.12, H, 3.17, N, 0.00. Found: C, 57.96, H, 2.95, N, 0.03.
EXAMPLE 14
[2,6-Dibromo-4-(dibenzothiophen-1-yl)-phenoxy]-acetic acid
To a solution of [2,6-dibromo-4-(dibenzothiophen-1-yl)-phenoxy]-acetic acid, ethyl ester (0.324 g, 0.623 mmol) in tetrahyodrofuran (15 mL) and methanol (5 mL) was added an aqueous solution of potassium hydroxide (1N, 0.75 mL, 0.75 mmol, 1.2 eq) dropwise at room temperature. After stirring 2.5 hours at room temperature the solvents were removed and the residue was combined with water (50 mL) and was acidified with 10% aqueous hydrochloric acid. After stirring 0.5 hours the white solid was filtered. Trituration with petroleum ether and recrystallization from aqueous acetic acid with hot filtration gave a white solid which was dried in vacuo at 100.degree. C. for 5 hours to provide the title compound as a white solid: (0.155 g, 51%); mp 212-213.degree. C.; NMR (DMSO-d6): .delta. 13.19 (broad s, 1H), 8.11 (dd, J=8, 1 Hz, 1H), 8.04 (dm, 1H), 7.78 (s, 2H), 7.55 (dd, J=8, 7 Hz, 1H), 7.45 (ddd, J=8, 7, 1 Hz, 1H), 7.31 (dd, J=7 Hz, 1H), 7.27 (ddd, J=8, 7, 1 Hz, 1H), 7.10 (dm, 1H), 4.67 (s, 2H); MS (+FAB): [M+], 2 bromine isotope pattern, 490 (61%), 492 (100%), 494 (57%); Anal. Calc. for C20H12Br2O3S: C, 48.81, H, 2.46, N, 0.00. Found: C, 48.99, H, 2.24, N, 0.07.
EXAMPLE 15
(S)-2-Hydroxy-3-phenylpropionic acid, methyl ester
A solution of commercially available (S)-2-hydroxy-3-phenylpropionic acid (5.0 g, 30.1 mmol) and p-toluenesulfonic acid hydrate (1g) in methanol (125 mL) was refluxed with removal of water using 3A molecular sieves for 17 h. The solution was concentrated and dissolved in ether. The ether solution was washed with saturated sodium bicarbonate, brine and concentrated to provide the title compound as a white solid (5.32 g, 98%): NMR (CDCl3): .delta. 7.36-7.20 (m, 5H), 4.47 (ddd, J=5, 6, 7 Hz, 1H), 3.78 (s, 3H), 3.14 (dd, J=5, 14 Hz, 1H), 2.97 (dd, J=7, 14 Hz), 2.69 (d, J=6 Hz, 1H).
EXAMPLE 16
(S)-(+)-.alpha.-Hydroxy-1,3-dioxo-2-isoindolinebutyric Acid, Methyl Ester
Prepared from commercially available (S)-(+)-.alpha.-hydroxy-1,3-dioxo-2-isoindolinebutyric acid according to the procedure in Example 9. White solid: mp 123-124.5: MS (EI): [M+], 263; Anal. Calc. for C13H13NO5: C 59.31, H, 4.98, N, 5.32. Found: C 59.04, H, 5.02, N, 5.06.
EXAMPLE 17
(R)-2-[2,6-Dibromo-4-(dibenzothiophen-1-yl)-phenoxy]-3-phenyl-propionic acid methyl ester
Diethylazodicarboxylate (DEAD, 0.077 mL, 1.15 mmol) was added to a stirred, room temperature suspension of 2,6-Dibromo-4-(dibenzothiophen-1-yl)-phenol (0.250 g, 0.576 mmol), (S)-2-hydroxy-3-phenylpropionic acid, methyl ester (0.208 g, 1.15 mmol), triphenylphosphine (0.302 g, 1.15 mmol) in benzene (3 mL) under a dry nitrogen atmosphere. Dissolution occurred and the solution was heated in an 80.degree. C. oil bath for 16 h. More diethylazodicarboxylate (DEAD, 0.039 mL, 0.576 mmol), (S)-2-hydroxy-3-phenylpropionic acid, methyl ester (0.104 g, 0.576 mmol) and triphenylphosphine (0.151 g, 0.576 mmol) were added and the solution was stirred an additional 4 h. Upon cooling to room temperature, the reaction mixture was diluted with ether and silica gel was added. The reaction mixture was concentrated and the silica adsorbate was flash chromatographed (98:2 petroleum ether:ethyl acetate) to provide the title compound as a white solid (0. 293 g, 85%): NMR (CDCl3): .delta. 7.89 (dd, J=8, 1 Hz, 1H), 7.85 (ddd., J=8, 1, 1 Hz, 1H), 7.64 (d, J=2 Hz, 1H), 7.63 (d, J=2 Hz, 1H), 7.47 (dd, J=9, 8 Hz, 2H), 7.41-7.17 (m, 8H), 5.13 (dd, J=8, 6 Hz, 1H), 3.71 (s, 3H), 3.55 (dd, J=7, 4 Hz, 1H), 3.53 (dd, J=8, 4 Hz, 1H); MS (EI): [M+], 2 bromine isotope pattern, 594 (20%), 596 (40%) 598 (25%); Anal. Calc. for C28H20Br2O3S: C, 56.39, H, 3.38, N, 0.00. Found: C, 56.27, H, 3.21, N, 0.09.
EXAMPLE 18
(R)-2-[2,6-Dibromo-4-(2-bromo-dibenzothiophen-1-yl)-phenoxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester
Diethylazodicarboxylate (0.300 mL, 1.91 mmol) was added dropwise to a stirred, ambient temperature suspension of 2,6-Dibromo-4-(6-bromo-dibenzothiophen-1-yl)-phenol (0.650 g, 1.27 mmol), (S)-(+)-2-hydroxy-1,3-dioxo-2-isoindolinebutyric acid, methyl ester (0.502 g, 1.912 mmol), triphenylphosphine (0.500 g, 1.91 mmol) and benzene (5 mL) under a dry nitrogen atmosphere. Dissolution occurred and the solution was heated in an 80.degree. C. oil bath for 7 h. Upon cooling to room temperature, the reaction mixture was diluted with dicloromethane and silica gel (10 mL) was added. The reaction mixture was concentrated and the silica adsorbate was flash chromatographed (75:25 petroleum ether:ethyl acetate) to provide the title compound as a white solid (0.564 g, 78 %): mp 99-101 .degree. C.; MS (FAB+): [M+H]+, 3 bromine isotope pattern, 756, 758, 760, 762.
EXAMPLE 19
(R)-2-[2,6-Dibromo-4-(dibenzothiophen-1-yl)-phenoxy]-3-phenyl-propionic acid
1.0 N Aqueous potassium hydroxide (0.81 mL, 0.81 mmol) was added to a stirred solution of (R)-2-[2,6-dibromo-4-(dibenzothiophen-1-yl)-phenoxy]-3-phenyl-propionic acid methyl ester (0.242 g, 0.406 mmol) in THF (4 mL) and methanol (2.5 mL). After 1.5 h at ambient temperature, the reaction mixture was diluted with water, acidified with 10% aqueous HCl and filtered. The solid was washed with water and triturated with pet. ether. The solid was dried in vacuo at 70.degree. C. to provide the title compound as a white solid (0.190, 80%): [a]D25=+19.73 (10.14 mg/mL CHCl3); NMR (CDCl3): .delta. 7.89 (dd, J=8, 1 Hz, 1H), 7.83 (ddd., J=8, 1, 1 Hz, 1H), 7.63 (d, J=2 Hz, 1H), 7.62 (d, J=2 Hz, 1H), 7.45 (dd, J=8, 6 Hz, 2H), 7.41-7.154 (m, 8H), 5.33 (t, J=8 Hz, 1H), 3.54 (dd, J=5, 2 Hz, 1H), 3.52 (dd, J=8, 4 Hz, 1H); MS (EI): [M+], 2 bromine isotope pattern, 580 (20%), 582 (40%) 584 (25%); Anal. Calc. for C27H18Br2O3S: C, 55.69, H, 3.11, N, 0.00. Found: C, 55.23, H, 2.97, N, 0.07; Analytical HPLC :98.8%.
EXAMPLE 20
(R)-2-[2,6-Dibromo-4-(2-bromo-dibenzothiophen-1-yl)-phenoxyl -3-phenyl-propionic acid
Diethylazodicarboxylate (0.276 nL, 1.76 mmol) was added dropwise to a stirred, room temperature solution of 2,6-Dibromo-4-(6-bromo-dibenzothiophen-1-yl)-phenol (0.60 g, 1.17 mmol), L-3-phenyllactic acid, methyl ester (0.316 g, 1.76 mmol), triphenylphosphine (0.46 g, 1.76 mmol) and benzene (5.5 mL) under a dry nitrogen atmosphere. The solution was heated in an 80.degree. C. oil bath for 6 h. Upon cooling to room temperature, the reaction mixture was diluted with dicloromethane and silica gel (18 mL) was added. The reaction mixture was concentrated and the silica adsorbate was flash chromatographed (93:7 petroleum ether:ethyl acetate) to provide a white solid (0.21 g, 85%): MS [EI], [M+], 672,674, 676, 678. Aqueous potassium hydroxide (1 N, 0.81 mL, 0.806 mmol) was added to a stirred solution of this methyl ester (0.495 g, 0.733 mmol) in THF (3 mL)/methanol (3 mL). After 6.5 h, the mixture was stirred at 50.degree. C. After 1.5 h., the solution was concentrated, diluted with water (100 mL) and acidified with 10% aqueous HCl. The solid was filtered, washed with water and triturated with petroleum ether to provide the title compound as a white solid (0.463 g, 90%): mp 98-100.degree. C.: NMR (CDCl3); .delta. 7.82 (ddd, J=8, 1, 1 Hz, 1H), 7.76 (d, J=9 Hz, 1H), 7.72 (d, J=9 Hz, 1H), 7.52 (d, J=1 Hz, 2H), 7.41-2.25 (m, 6 H), 7.14 (ddd, J=8, 7, 1 Hz, 1H), 6.69 (dd, J=8, 1 Hz, 1H), 5.37 (t, J=7 Hz, 1H), 3.53 (d, J=7 Hz, 2H) MS (+FAB): [M+], 3 bromine isotope pattern, 658, 660, 662,664; Anal. Calc. for C27H17Br3O3S: C 49.05, H, 2.59, N, 0.00. Found: C 49.49, H, 2.54, N, 0.13.
EXAMPLE 21
(R)-2-[2,6-Dibromo-4-(2-bromo-dibenzothiophen-1-yl)-phenoxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid
A solution of (R)-2-[2,6-dibromo-4-(2-bromo-dibenzothiophen-1-yl)-phenoxy]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyric acid methyl ester (0.514 g, 0.68 mmol) and lithium iodide (0.915 g, 6.8 mmol) in pyridine (20 mL) was stirred at 110.degree. C. After 2 days, the mixture was quenched with 10% aqueous HCl and further diluted with water (150 mL). Aqueous mixture was extracted with dichloromethane (150 mL). The dichloromethane extract was washed with water, dried with brine. Silica gel was added. Solvent was removed and the adsorbate was flash chromatographed (eluent 7:3 petroleum ether:ethyl acetate) to provide the title compound as a white solid (0.319 g, 63%): mp 130-132.degree. C.: NMR (CDCl3): .delta. 7.86 (dd, J=8, 1 Hz, 2H), 7.81 (d, J=8 Hz, 1H), 7.77-7.70 (m, 4 H), 7.52 (d, J=1 Hz, 2H), 7.39 (ddd, J=8, 7, 1 Hz, 1H), 7.18 (ddd, J=8, 7, 1 Hz, 1H), 6.77 (d, J=8 Hz, 1H), 5.24 (t, J=7 Hz, 1H), 4.21-4.05 (m, 2 H), 2.67-2.55 (m, 2H); MS (+EI): [M+], 3 bromine isotope pattern, 741, 743, 745, 747; Anal. Calc. for C3OH18Br3NO5S: C 48.86, H, 2.74, N, 1.83. Found: C 48.90, H, 2.82, N, 1.18.

1-aryl-dibenzothiophenes

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