WO1998032436A1 - Treatment for premenstrual dysphoric disorder - Google Patents
Treatment for premenstrual dysphoric disorder Download PDFInfo
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- WO1998032436A1 WO1998032436A1 PCT/US1998/001344 US9801344W WO9832436A1 WO 1998032436 A1 WO1998032436 A1 WO 1998032436A1 US 9801344 W US9801344 W US 9801344W WO 9832436 A1 WO9832436 A1 WO 9832436A1
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- hexane
- mmol
- dicarboxylic acid
- agonist
- amino
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- 0 C[C@@](C1*C2)[C@]1C2O Chemical compound C[C@@](C1*C2)[C@]1C2O 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
Definitions
- the present invention relates to the treatment of premenstrual dysphoric disorder.
- Premenstrual dysphoric disorder is described on pages 715 to 718 of the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DMS-IV) , published by the American Psychiatric Association, Washington, DC, 1994.
- the condition is characterized by at least one of a markedly depressed mood, marked anxiety, marked affective ability and decreased interest m activities.
- These symptoms develop during the last week of the luteal phase of a menstrual cycle, and begin remission within a few days of the onset of the follicular phase (menses) .
- Other symptoms which may develop are irritability, lack of concentration, fatigue, appetite change, disruption of normal sleep patterns, a sense of being out of control and physical symptoms such as breast tenderness or swelling, weight gain and pains.
- Females suffering from premenstrual dysphoric disorder commonly experience difficulties with personal relationships and m their obs or schooling. Sometimes the symptoms are accompanied by thoughts of suicide. The condition is not restricted to menstruating females, and may also occur m non-menstruating females undergoing a cycle of luteal and follicular phases, for example females who have had a hysterectomy .
- premenstrual dysphoric disorder is distinguishable from the premenstrual exacerbation of current mental disorders such as mood disorders and anxiety disorders.
- the latter disorders persist throughout the menstrual cycle, although the symptoms may present most acutely during the premenstrual phase .
- the present invention provides a method of treating premenstrual dysphoric disorder, which comprises administering to a female subject in need of treatment an effective amount of an agonist which acts at negatively- coupled cAMP-linked metabotropic glutamate receptors.
- the present invention provides the use of an agonist which acts at negatively coupled cAMP-linked metabotropic glutamate receptors for the manufacture of a medicament for the treatment of premenstrual dysphoric disorder.
- the present invention provides a pharmaceutical composition for use in the treatment of premenstrual dysphoric disorder, which comprises an agonist which acts at negatively-coupled cAMP- linked metabotropic glutamate receptors.
- the particular dose of agonist administered according to this invention will of course be • determined by the particular circumstances surrounding the case, including the activity of the particular agonist administered, the route of administration, the particular condition being treated, and similar considerations.
- the agonist can be administered by a variety of routes including oral, rectal, transdermal, subcutaneous, intravenous, intramuscular, or intranasal routes. Alternatively, the agonist may be administered by continuous infusion.
- a typical daily dose will contain from about 0.001 mg/kg to about 100 mg/kg of the agonist.
- daily doses will be about 0.05 mg/kg to about 50 mg/kg, more preferably from about 0.1 mg/kg to about 20 mg/kg .
- the agonist is preferably formulated prior to administration in combination with one or more pharmaceutically-acceptable carriers, diluents, or excipients .
- the pharmaceutical formulations are prepared by known procedures using well-known and readily available ingredients.
- the active ingredient will usually be mixed with a carrier, or diluted by a carrier, or enclosed within a carrier, and may be in the form of a capsule, sachet, paper, or other container.
- the carrier serves as a diluent, it may be a solid, semi-solid, or liquid material which acts as a vehicle, excipient, or medium for the active ingredient.
- compositions can be in the form of tablets, pills, powders, lozenges, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols, ointments containing, for example, up to 10% by weight of active compound, soft and hard gelatin capsules, suppositories, sterile injectable solutions, dermal patch, subcutaneous implant, and sterile packaged powders .
- Suitable carriers, excipients, and diluents include lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum, acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water syrup, methyl cellulose, methyl and propyl hydroxybenzoates , talc, magnesium stearate, stearic acid, and mineral oil.
- the formulations can additionally include lubricating agents, wetting agents (surfactants), emulsifying and suspending agents, preserving agents, sweetening agents, or flavoring agents.
- compositions may be formulated so as to provide quick, sustained, or delayed release of the active ingredient after administration to the patient by employing procedures well known in the art.
- the compositions are preferably formulated in a unit dosage form, each dosage containing from about 1 mg to about 500 mg, more preferably about 5 mg to about 200 mg of the active ingredient.
- unit dosage form refers to a physically discrete unit suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical carrier, diluent, or excipient .
- the following formulation examples are illustrative only and are not intended to limit the scope of the invention in any way .
- Tablets each containing 60 mg of agonist are made as follows :
- the agonist, starch, and cellulose are passed through a No. 45 mesh U.S. sieve and mixed thoroughly.
- the solution of polyvinylpyrrolidone is mixed with the resultant powders which are then passed through a No . 14 mesh U.S. sieve.
- the granules so produced are dried at 50°C and passed through a No. 18 mesh U.S. sieve.
- the sodium carboxymethyl starch, magnesium stearate, and talc previously passed through a No. 60 mesh U.S. sieve, are then added to the granules which, after mixing, are compressed on a tablet machine to yield tablets each weighing 150 mg.
- Capsules each containing 80 mg of agonist are made as follows :
- the active ingredient, cellulose, starch, and magnesium stearate are blended, passed through a No . 45 sieve, and filled into hard gelatin capsules in 200 mg quantities.
- Agonists which act at negatively coupled cAMP-linked metabotropic glutamate receptors may be identified using the following experiment. Firstly, the affinity of a test compound for metabotropic glutamate receptors may be demonstrated by the selective displacement of (lS,3i?)-l- aminocyclopentane-1 , 3-dicarboxylic acid-sensitive
- the affinity of a test compound for the receptor may be expressed as the concentration of the test compound that inhibits 50% binding (IC50), or the percent displacement of [- ⁇ HJGlu at a 10 ⁇ M or 100 ⁇ M concentration of the formula I compound.
- test compounds The ability of a test compound to act as an agonist at negatively coupled cAMP-linked metabotropic receptors may be measured using the following method. Test compounds are tested for their ability to decrease forskolin-stimulated cAMP formation in the rat hippocampus and the rat cerebral cortex, using the procedures described in Schoepp and Johnson. Schoepp and Johnson, Neurochem . Int . , 22, 277-283 (1993) .
- the women have regular menses, are in good general health, and suffer from one or more of the above mentioned PMS symptoms. Because of the somewhat idiosyncratic and subjective nature of these symptoms, the study has a placebo control group, i.e., the women are divided into two groups, one of which receives the agonist (the active agent of this invention), and the other receives a placebo. Women in the test group receive between 10-400 mg of the drug per day by the oral route. They continue this therapy for 1-3 months. Accurate records are kept as to the number and severity of the symptoms in both groups and at the end of the study these results are compared. The results are compared both between members of each group and also the results for each patient are compared to the symptoms reported by each patient before the study began.
- the effectiveness of the invention is illustrated by the positive impact observed on one or more of the symptoms of premenstrual dysphoric disorder in a study as described above .
- the agonist which acts at negatively-coupled cAMP- linked metabotropic glutamate receptors may be a compound of the formula
- X represents CH2 , 0 or S, or a pharmaceutically acceptable metabolically labile ester or amide thereof, or a pharmaceutically acceptable salt thereof.
- Preferred compounds of formula I are:
- R- ⁇ -0 represents a hydrogen atom or an acyl group and R ⁇ represents a carboxyl group or an esterified carboxyl group, or a salt thereof;
- R ⁇ represents a carboxyl group or an esterified carboxyl group
- RU and ⁇ A-2 each independently represent a hydrogen atom, a (2-6C) alkanoyl group, a (1-4C) alkyl group, a (3-4C) alkenyl group or a phenyl (1-4C) alkyl group in which the phenyl is unsubstituted or substituted by halogen, (1-4C) alkyl or (1- 4C) alkoxy, or a salt thereof; or
- R 1 ⁇ represents a hydrogen atom or a nitrogen protecting group and each of R ⁇ 3 and R ⁇ -4 independently represents a hydrogen atom or a carboxyl protecting group, or a salt thereof;
- carboxy protecting groups include alkyl groups such as methyl, ethyl, t-butyl and t- a yl; aralkyl groups such as benzyl, 4-nitrobenzyl , 4- methoxybenzyl , 3 , 4-dimethoxybenzyl , 2 , 4-dimethoxybenzyl , 2 , 4 , 6-trimethoxybenzyl , 2 , 4 , 6-trimethylbenzyl , benzhydryl and trityl; silyl groups such as trimethylsilyl and t- butyldimethylsilyl ; and allyl groups such as allyl and 1- ( trimethylsilylmethyl ) prop-l-en-3-yl .
- alkyl groups such as methyl, ethyl, t-butyl and t- a yl
- aralkyl groups such as benzyl, 4-nitrobenzyl , 4- methoxybenzyl ,
- amine protecting groups include acyl groups, such as groups of formula R 1:L CO in which R 11 represents (1-6C) alkyl, (3-10C) cycloalkyl, phenyl (1-6C) alkyl, phenyl, (1-6C) alkoxy, phenyl (1-6C) alkoxy , or a (3-10C) cycloalkoxy, wherein a phenyl group may optionally be substituted by one or two substituents independently selected from amino, hydroxy, nitro, halogeno, (1-6C) alkyl, (1-6C) alkoxy, carboxy, (1- 6C) alkoxycarbonyl , carbamoyl, (1-6C) alkanoylamino, (1-6C) alkylsulphonylamino, phenylsulphonylamino, toluenesulphonyl- amino, and (1-6C) fluoroalkyl .
- R 11 represents (1-6C) alkyl, (3-10C)
- the compounds of formula II are conveniently hydrolyzed in the presence of an acid, such as hydrochloric acid or sulfuric acid, or a base, such as an alkali metal hydroxide, for example sodium hydroxide.
- the hydrolysis is conveniently performed in an aqueous solvent such as water and at a temperature in the range of from 50 to 200_C.
- the compounds of formula III are conveniently hydrolyzed in the presence of a base, for example an alkali metal hydroxide such as lithium, sodium or potassium hydroxide, or an alkaline earth metal hydroxide such as barium hydroxide.
- a base for example an alkali metal hydroxide such as lithium, sodium or potassium hydroxide, or an alkaline earth metal hydroxide such as barium hydroxide.
- Suitable reaction media include water.
- the temperature is conveniently in the range of from 50 to 150 °C.
- R!0 is hydrogen and (2- 6C) alkanoyl groups, such as acetyl .
- R ⁇ when it represents an esterified carboxyl group are ( 1-6C) alkoxycarbonyl groups such as ethoxycarbonyl .
- the compounds of formula IV may be deprotected by a conventional method.
- an alkyl carboxyl protecting group may be removed by hydrolysis.
- the hydrolysis may conveniently be performed by heating the compound of formula V in the presence of either a base, for example an alkali metal hydroxide such as lithium, sodium or potassium hydroxide, or an alkaline metal hydroxide, such as barium hydroxide, or an acid such as hydrochloric acid.
- the hydrolysis is conveniently performed at a temperature in the range of from 10 to 300 °C.
- An aralkyl carboxyl protecting group may conveniently be removed by hydrogenation .
- the hydrogenation may conveniently be effected by reacting the compound of formula V with hydrogen in the presence of a Group VIII metal catalyst, for example a palladium catalyst such as palladium on charcoal.
- a Group VIII metal catalyst for example a palladium catalyst such as palladium on charcoal.
- Suitable solvents for the reaction include alcohols such as ethanol .
- the reaction is conveniently performed at a temperature in the range of from 0 to 100 C.
- An acyl, amine protecting group is also conveniently removed by hydrolysis, for example as described for the removal of an alkyl carboxyl protecting group.
- the compounds of formula II may be prepared by reacting a compound of formula V
- an alkali metal cyanide such as lithium, sodium or potassium cyanide
- an ammonium halide such as ammonium chloride
- the ammonium halide is mixed with chromatography grade alumina in the presence of a suitable diluent such as acetonitrile .
- the mixture is then irradiated with ultrasound, whereafter the compound of formula V is added, and the mixture is again irradiated.
- the alkali metal cyanide is then added, followed by further irradiation with ultrasound.
- the resultant mixture of diastereoisomeric aminonitriles is then reacted with an acylating agent, such as acetyl chloride in the presence of a suitable base, for example an amine such as ethyl diisopropylamine and in the presence of a suitable solvent, such as dichloromethane, to afford a mixture of diastereomeric acylamino nitriles.
- an acylating agent such as acetyl chloride
- a suitable base for example an amine such as ethyl diisopropylamine
- a suitable solvent such as dichloromethane
- the compounds of formula III may be prepared by reacting a compound of formula V with an alkali metal cyanide, such as lithium, sodium or potassium cyanide, and ammonium carbonate or ammonium carbamate.
- alkali metal cyanide such as lithium, sodium or potassium cyanide
- ammonium carbonate or ammonium carbamate include alcohols, such as methanol, aqueous methanol and aqueous ethanol . Conveniently the reaction is performed at a temperature in the range of from 10 to 150°C. If desired, the compounds of formula III may then be alkylated, for example using an appropriate compound of formula R l Cl and/or R 1 C1.
- the compounds of formula III may conveniently be resolved prior to hydrolysis.
- a compound of formula III in which R ⁇ represents a carboxyl group may be resolved by treatment with an optically active amine, such as (R) -2-phenylglycinol .
- the compounds of formula V in which X represents 0 may be prepared by cyclising a compound of formula
- Z ⁇ represents a leaving atom or group, for example an iodine atom.
- the reaction is conveniently performed in the presence of a base, such as 1,8- diazabicyclo [5.4.0] undec-7-ene .
- Suitable solvents include ethers, such as tetrahydrofuran.
- the temperature is conveniently in the range of from 0 to 100_C.
- the compounds of formula VI may be prepared by oxidising a compound of formula
- the oxidation is conveniently effected using an appropriate conventional oxidation method, for example, using oxalyl chloride in dimethyl sulfoxide or (when X is 0 only) chromium trioxide in sulfuric acid (Jones reagent) .
- the compounds of formula Via may be prepared by the method described in J. Amer . Chem. Soc, 110 (14), 1988, pages 4533-4540.
- the compound of formula V may also be prepared by oxidizing a compound of formula
- the oxidation may conveniently be effected by reacting the compounds of formula VII with dimethyl sulfoxide in the presence of an activating agent, such as oxalyl chloride, followed by treatment with a base, such as triethylamine .
- an activating agent such as oxalyl chloride
- a base such as triethylamine
- the compounds of formula VII may be prepared by reacting a compound of formula
- reaction may generally be performed according to the methods described in J. Am. Chem. Soc. 1986, 108, 2049 and J. Am. Chem. Soc, 1991, 113, 4037.
- the compounds of formula IX may be prepared by reacting a compound of formula
- reaction may generally be performed according to the methods described in J. Chem. Soc. Perkin Tran I, 1979, 2624; Tetrahedron, 1971, 27, 2957. Justus Liebigs Ann. Chem. 1963, 668, 19; and Tet . Let. 1964, 2185.
- a transition metal catalyst such as a rhodium or copper catalyst.
- step (c) 5SR.E-Ethyl ⁇ SR, E) 5 , 6-Dihydroxy-2 -hexenoate .
- a solution of the product of step (b) (46.4 g, 216.6 mmol) in THF (700 mL) was treated in one portion with IN HCl (500 mL) and stirred at ambient temperature overnight .
- EtOAc and NaCl were added and the resulting slurry stirred vigorously for two hours.
- the reaction mixture was partitioned in a separatory funnel and the product extracted with EtOAc . All organics were combined, washed with brine, dried over MgS ⁇ 4, and concentrated in vacuo to yield the crude diol .
- step (e) 2SR-Ethyl 2- [ (4-oxo-tetrahydrofuran-2-yl ) ] -iodoacetate .
- a solution of the product of step (d) (28.5 g, 95 mmol) in CH 2 CI 2 (500 mL) with 3A sieves was treated in one portion with pyridinium chlorochromate (91.5 g, 425 mmol) and stirred at ambient temperature overnight .
- the reaction mixture was diluted with Et 2 ⁇ and filtered through celite ® .
- step (f) 1SR,5SR, 6SR-Ethyl 2-oxabicyclo [3.1.0] hexan-4-one-6- carboxylate.
- a solution of the product of step (e) (5.25 g, 17.6 mmol) in THF (50 mL) was treated by dropwise addition of a solution DBU (2.82 g, 18.5 mmol) in THF (10 mL) and the resulting reaction mixture stirred at ambient temperature for 1 hour.
- the reaction mixture was reduced in vacuo, partitioned between Et 2 ⁇ and IN HCl, and the product extracted with Et 2 ⁇ . All organics were combined, washed with brine, dried over MgS0 4 , and concentrated in vacuo to yield the crude product.
- step (g) 1SR, 4SR, 5RS, 6SR-Diethyl 4- (a inobenzyloxycarbonyl) -2- oxabicyclo [3.1.0] - hexane-4 , 6-dicarboxylate .
- a solution of the product of step (f) (3.0 g, 17.6 mmol) in a 1:1 mixture of EtOH:H 2 ⁇ (50 mL total volume) was treated consecutively with NH 2 CO 2 NH 4 (4.13 g, 52.9 mmol), then KCN (1.72 g, 26.4 mmol) and warmed at 55°C for 40 hours.
- NaOH 4.0 g, 100 mmol
- the reaction mixture was concentrated in vacuo and the crude aminodiacid reconstituted in H 2 O .
- the solids were reconstituted in a 1:1 mixture of THF:H 2 ⁇ (100 mL total volume) , stirred at 0°C as benzylchloroformate (4.50 g, 26.4 mmol) was added dropwise, and allowed to warm to ambient temperature as it stirred for 48 hours.
- the reaction mixture was diluted and washed with Et 2 ⁇ .
- the product was extracted with EtOAc, dried over MgS04 , and concentrated in vacuo to yield the crude N-CBZ diacid.
- This intermediate was reconstituted in CH 3 CN and treated consecutively with triethylamine (5.6 g 56 mmol) then iodoethane (6.5 g, 42 mmol) and warmed at 50°C for 48 hours.
- the reaction mixture was diluted with Et 2 ⁇ and partitioned with IN HCl.
- H20 C, 49.16; H, 6.60; S, 16.40. Found: C, 49.03; H, 6.28; S, 17.80.
- step (b) Upon complete addition the reaction was allowed to equilibrate for 30 minutes, followed by dropwise addition of a solution of the product of step (b) (4.31 g, 22.8 mmol) in CH2CI2 (20 mL) maintaining reaction temperature 2 -65°C.
- step (e) ( 1SR, 4RS, 5RS, 6RS) 4-Amino [2-thiabicyco [3.1.0] hexane] - 4 , 6-dicarboxylate .
- a solution of the product from step (d) (0.85 g, 3.30 mmol) in 2N NaOH (20 mL) was warmed under reflux for 4 days. The reaction mixture was then acidified with 6N HCl and concentrated to dryness . The solid was
- step (a) 32.73 g, 212.30 mmol was dissolved in 150 mL of THF under N2 •
- the resultant solution was cooled with stirring to -0.5°C. While the stirring solution was cooling, the system was evacuated and purged with N2 twice.
- the entire thexylborane solution prepared above was added via cannula over 40 minutes, maintaining the temperature ⁇ 4.4°C.
- 87 mL of 30% H2O2 was added slowly, over 70 minutes, to maintain the temperature at ⁇ 30°C.
- the aqueous layer was back extracted three times with 50 mL of EtOAc.
- the combined organic layers were washed with 30 mL of brine and dried over Na2S04.
- the solvent was removed to afford 54.44 g of an oil.
- the oil was purified by a flash chromatography (370 g of silica gel, wet packed with 3:2 hexanes : EtOAc) eluting with 3:2 hexanes : EtOAc, to afford 31.72 g of the title compound as an oil.
- the aqueous layer was back extracted with 50 mL of CH2CI2 • The combined organic layers were washed with 75 mL of brine and dried over Na2S04. Most of the solvent was removed by rotary evaporation to leave 44.36 g of liquid. A few seed crystals were added and the flask was blanketed with N2 and stirred ambient temperature for 30 minutes while a thin slurry formed. To the room temperature slurry was slowly added 20 L of hexanes . The slurry was stirred 90 minutes at ambient temperature then 3 hours in an ice/NaCl/water bath.
- the pH was adjusted from 9.6 to 7.0 with 6 N hydrochloric acid giving a white solid.
- the slurry was stirred at 0-5°C for 1.5 hours, filtered and washed with 75 mL of cold water-methanol (2:1) .
- the white solid was dried in vacuo at 40°C affording the title compound (5.55 g, 78.6%).
- the product was identified by 1 H NMR.
- step (f) 1R, 4R, 5S, 6R- (-) -4-spiro-5 ' -hydantoin-2- oxabicyclo [3.1.0] hexane carboxylic acid, (R)-(-)-2- phenylglycinol salt.
- step (e) (0.80 g, 3.8 mmol) was added (R) - ( - ) -phenylglycinol (0.52 g, 3.8 mmol) in ethanol (20 mL) and water (4 mL) .
- the mixture was heated to reflux, and an additional 1 mL of water was added, producing a homogenous solution. After approximately 30 minutes at reflux, the mixture was allowed to cool to ambient temperature.
- step (g) 1R, 4R, 5S, 6R- (-) -4-Amino-2 -oxabicyclo [3.1.0]hexane- 4, 6-dicarboxylic acid.
- step (f) 1.0 g, 2.86 mmol
- 2M aqueous sodium hydroxide 15 mL (30 mmol, 10 eq)
- the solution was heated at reflux for 43 hours.
- the resulting mixture was allowed to cool to ambient temperature, then extracted with CH2CI2 (5 x 30 mL) .
- the aqueous layer was diluted with lO L of H2O and acidified to pH2 with 3M HCl.
- the cloudy mixture was filtered, and the pH was adjusted to 8 using 2M NaOH, then the solution was allowed to stand over the weekend. This resulted in formation of a gel from the remaining silicic acid.
- the gel was removed by filtration through a medium glass frit over 1 hour and rinsed with 50 mL of H2O.
- An ion exchange column was prepared from 25 g of Bio- Rad AG 1-X8-, 100-200 mesh, acetate form, resin.
- the resin was transferred to a gravity flow column using deionized H2O and washed sequentially with 1M NaOH (2 x 50 mL) and H2O (2 x 50 mL or until eluent neutral) .
- the aqueous product solution was poured onto the resin in 50 mL portions.
- the column was washed sequentially with H2O until the eluent was neutral (about 100 mL) , 70 mL of 1:1 THF/H2O, and 100 mL of H2O.
- the product was eluted with 120 mL of a 1:3 mixture of acetic acid and H2O. The entire eluent was collected in one flask and evaporated to 0.48 g of a white solid. The solid was slurried in 5 mL of H2O and collected on a coarse glass frit. The flask was rinsed with additional H2O (2 x 5 mL) and these rinsings were used to wash the collected solid. After drying under vacuum at 70°C for 18 hours, the title compound (0.33 g, 62%) was obtained as a white solid. The structure was confirmed by ⁇ H NMR and analysis.
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Abstract
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53215898A JP2001511131A (en) | 1997-01-29 | 1998-01-23 | Treatment of premenstrual discomfort |
CA002275777A CA2275777A1 (en) | 1997-01-29 | 1998-01-23 | Treatment for premenstrual dysphoric disorder |
AU62487/98A AU6248798A (en) | 1997-01-29 | 1998-01-23 | Treatment for premenstrual dysphoric disorder |
EP98904669A EP1014971A1 (en) | 1997-01-29 | 1998-01-23 | Treatment for premenstrual dysphoric disorder |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US3617697P | 1997-01-29 | 1997-01-29 | |
US60/036,176 | 1997-01-29 |
Publications (1)
Publication Number | Publication Date |
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WO1998032436A1 true WO1998032436A1 (en) | 1998-07-30 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US1998/001344 WO1998032436A1 (en) | 1997-01-29 | 1998-01-23 | Treatment for premenstrual dysphoric disorder |
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EP (1) | EP1014971A1 (en) |
JP (1) | JP2001511131A (en) |
AU (1) | AU6248798A (en) |
CA (1) | CA2275777A1 (en) |
WO (1) | WO1998032436A1 (en) |
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WO2011122701A1 (en) * | 2010-03-29 | 2011-10-06 | Vanderbilt University | Method for treating schizophrenia and related diseases |
US8058474B2 (en) | 2003-11-11 | 2011-11-15 | Eisai R&D Management Co., Ltd. | Urea derivative and process for preparing the same |
US8865737B2 (en) | 2006-08-28 | 2014-10-21 | Eisai R&D Management Co., Ltd. | Antitumor agent for undifferentiated gastric cancer |
US8952035B2 (en) | 2007-11-09 | 2015-02-10 | Eisai R&D Management Co., Ltd. | Combination of anti-angiogenic substance and anti-tumor platinum complex |
US8962655B2 (en) | 2007-01-29 | 2015-02-24 | Eisai R&D Management Co., Ltd. | Composition for treatment of undifferentiated gastric cancer |
US8962650B2 (en) | 2011-04-18 | 2015-02-24 | Eisai R&D Management Co., Ltd. | Therapeutic agent for tumor |
US8969379B2 (en) | 2004-09-17 | 2015-03-03 | Eisai R&D Management Co., Ltd. | Pharmaceutical compositions of 4-(3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy)-7=methoxy-6-quinolinecarboxide |
US8969344B2 (en) | 2005-08-02 | 2015-03-03 | Eisai R&D Management Co., Ltd. | Method for assay on the effect of vascularization inhibitor |
US9006256B2 (en) | 2006-05-18 | 2015-04-14 | Eisai R&D Management Co., Ltd. | Antitumor agent for thyroid cancer |
US9012458B2 (en) | 2010-06-25 | 2015-04-21 | Eisai R&D Management Co., Ltd. | Antitumor agent using compounds having kinase inhibitory effect in combination |
US9334239B2 (en) | 2012-12-21 | 2016-05-10 | Eisai R&D Management Co., Ltd. | Amorphous form of quinoline derivative, and method for producing same |
US9945862B2 (en) | 2011-06-03 | 2018-04-17 | Eisai R&D Management Co., Ltd. | Biomarkers for predicting and assessing responsiveness of thyroid and kidney cancer subjects to lenvatinib compounds |
US10259791B2 (en) | 2014-08-28 | 2019-04-16 | Eisai R&D Management Co., Ltd. | High-purity quinoline derivative and method for manufacturing same |
US10517861B2 (en) | 2013-05-14 | 2019-12-31 | Eisai R&D Management Co., Ltd. | Biomarkers for predicting and assessing responsiveness of endometrial cancer subjects to lenvatinib compounds |
US11090386B2 (en) | 2015-02-25 | 2021-08-17 | Eisai R&D Management Co., Ltd. | Method for suppressing bitterness of quinoline derivative |
US11369623B2 (en) | 2015-06-16 | 2022-06-28 | Prism Pharma Co., Ltd. | Anticancer combination of a CBP/catenin inhibitor and an immune checkpoint inhibitor |
US11547705B2 (en) | 2015-03-04 | 2023-01-10 | Merck Sharp & Dohme Llc | Combination of a PD-1 antagonist and a VEGF-R/FGFR/RET tyrosine kinase inhibitor for treating cancer |
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- 1998-01-23 AU AU62487/98A patent/AU6248798A/en not_active Abandoned
- 1998-01-23 CA CA002275777A patent/CA2275777A1/en not_active Abandoned
- 1998-01-23 EP EP98904669A patent/EP1014971A1/en not_active Withdrawn
- 1998-01-23 JP JP53215898A patent/JP2001511131A/en active Pending
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EP0696577A1 (en) * | 1994-08-12 | 1996-02-14 | Eli Lilly And Company | Synthetic excitatory amino acids |
WO1996004901A1 (en) * | 1994-08-12 | 1996-02-22 | Eli Lilly And Company | Composition and method for treating anxiety |
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US8735397B2 (en) | 2010-03-29 | 2014-05-27 | Vanderbilt University | Method for treating schizophrenia and related diseases |
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US8962650B2 (en) | 2011-04-18 | 2015-02-24 | Eisai R&D Management Co., Ltd. | Therapeutic agent for tumor |
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US10822307B2 (en) | 2014-08-28 | 2020-11-03 | Eisai R&D Management Co., Ltd. | High-purity quinoline derivative and method for manufacturing same |
US11186547B2 (en) | 2014-08-28 | 2021-11-30 | Eisai R&D Management Co., Ltd. | High-purity quinoline derivative and method for manufacturing same |
US10407393B2 (en) | 2014-08-28 | 2019-09-10 | Eisai R&D Management Co., Ltd. | High-purity quinoline derivative and method for manufacturing same |
US11090386B2 (en) | 2015-02-25 | 2021-08-17 | Eisai R&D Management Co., Ltd. | Method for suppressing bitterness of quinoline derivative |
US11547705B2 (en) | 2015-03-04 | 2023-01-10 | Merck Sharp & Dohme Llc | Combination of a PD-1 antagonist and a VEGF-R/FGFR/RET tyrosine kinase inhibitor for treating cancer |
US11369623B2 (en) | 2015-06-16 | 2022-06-28 | Prism Pharma Co., Ltd. | Anticancer combination of a CBP/catenin inhibitor and an immune checkpoint inhibitor |
Also Published As
Publication number | Publication date |
---|---|
AU6248798A (en) | 1998-08-18 |
EP1014971A4 (en) | 2000-07-05 |
JP2001511131A (en) | 2001-08-07 |
EP1014971A1 (en) | 2000-07-05 |
CA2275777A1 (en) | 1998-07-30 |
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