Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
  • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
  • C07D491/04—Ortho-condensed systems
• • 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
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents

Definitions

• the present invention relates to a novel compound having antitumor activity, a process for producing the compound, and an antitumor agent containing the compound as an active ingredient.
• an object of the present invention is to provide a novel compound having antitumor activity, a process for producing the compound, and an antitumor agent containing the compound as an active ingredient.
• the inventors of the present invention have devoted themselves to the study for attaining the above object and have completed the present invention by finding out a novel compound having antitumor activity.
• R represents a linear, branched, or cyclic alkyl or aryl group.
• Preferred embodiment of the present invention is a compound wherein R in the general formula (I) is a linear, branched, or cyclic alkyl group.
• Preferred embodiment of the present invention is a compound wherein R in the general formula (I) is a linear, branched, or cyclic alkyl group having 1 to 6 carbon atoms.
• Preferred embodiment of the present invention is a compound wherein R in the general formula (I) is a tert-butyl group.
• Preferred embodiment of the present invention is a novel compound represented by the following formula (II).
• the present invention provides a process for producing a compound represented by the general formula (I), comprising:
• R and X each represent a linear, branched, or cyclic alkyl or aryl group
• the present invention provides a process for producing a compound represented by the general formula (III), comprising
• the present invention further provides a pharmaceutical agent containing a novel compound represented by the general formula (I) as an active ingredient.
• a pharmaceutical agent containing a novel compound represented by the general formula (I) as an active ingredient.
• said pharmaceutical agent is an antitumor agent.
• a compound of the present invention is that represented by the following general formula (I):
• R represents a linear, branched, or cyclic alkyl or aryl group.
• R represents a linear, branched, or cyclic alkyl or aryl group, and preferably a linear, branched, or cyclic alkyl or aryl group such as a phenyl group, having 1 to 6 carbon atoms, more preferably a linear or branched alkyl group having 1 to 6 carbon atoms.
• a methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, n-pentyl group, n-hexyl group, phenyl group, or the like can be used, with a tert-butyl group being preferred.
• the compound of the present invention represented by the general formula (I) has several asymmetric carbons, or may additionally have one or more asymmetric carbons depending on the type of a substituent. While stereoisomers such as optical isomers and diastereoisomers based on such an asymmetric carbon exist, mixtures of any stereoisomers or racemic bodies, in addition to stereoisomers in pure form, are included in the scope of the present invention. Moreover, the compound of the present invention has an olefinic double bond. While there are geometric isomers based on a double bond, mixtures of any geometric isomers, in addition to geometric isomers in pure form, are included in the scope of the present invention.
• the compound of the present invention may exist as a tautomer, any tautomers or mixtures thereof are included in the scope of the present invention.
• the compound of the present invention can take any crystal form in one form.
• the compound can exist as a hydrate or a solvate.
• the compound of the present invention can exist as a pharmaceutically acceptable salt in another form.
• Each form can be converted into a preferable form by standard manners depending on the purpose of the usage. It is obvious that any of those materials is included in the scope of the present invention.
• a producing process of the present invention is a process for producing the compound represented by the general formula (I).
• the producing process of the present invention preferably used is, but not limited to, for example a pathway indicated in Synthesis Scheme 1 described below.
• Acids, bases, catalysts, solvents, reaction temperatures, reaction times, and so on employed in the reaction pathway shown in Synthesis Scheme 1 can be appropriately altered based on organic synthesis approaches which are generally well known. Thus, methods including such alteration pertain to the scope of the producing process according to the present invention.
• the corresponding compound represented by the general formula (I) can be produced by replacing a t-butyl portion of phosphonoacetate used in the Horner-Emmons reaction of the transformation process from Compound 6 to Compound 7 in Synthesis Scheme 1, with a suitable substituent for the desired compound represented by the general formula (I).
• DIBAL-H diisobutylaluminium hydride
• HMPA hexamethylphosphoramide
• TrOOH tritylperoxide
• R and X each represent a linear, branched, or cyclic alkyl or aryl group.
• Compound (A) can be synthesized, for example, as follows.
• tert-butyl diethyl phosphonoacetate of a variety of esters of phosphonoacetic acid can be obtained as follows.
• Triethyl phosphite (24 cc) is added to t-butyl-2-bromopropanate (27.3 g), followed by stirring at 160° C. for 20 minutes. Distillation under reduced pressure is performed to produce tert-butyl diethyl phosphonoacetate (32 g; 91%).
• 2-(triethylsiloxy) propanal can be synthesized, for example, as follows.
• Triethylsilyl chloride is added to a DMF solution of methyl lactate and imidazole and the whole is stirred at room temperature.
• Methyl 2-triethylsiloxy propanoate is obtained by isolation and purification using methods generally used for isolating and purifying organic compounds.
• Methyl 2-triethylsiloxy propanoate is reduced with isobutylaluminium hydride and 2-triethylsiloxy-1-propanol is obtained by isolation and purification using methods generally used for isolating and purifying organic compounds.
• 2-triethylsiloxy-1-propanol is oxidized with an oxidizing agent such as SO 3 -pyridine in the presence of a base to produce Compound (C).
• Compound 4 can be obtained by protecting a free hydroxyl group of Compound 3 with an appropriate protecting group such as a TBDPS group, TBDMS (TBS) group, TES group, TIPS group, DMES group, THP group, EE group, MOM group, or Bn group.
• an appropriate protecting group such as a TBDPS group, TBDMS (TBS) group, TES group, TIPS group, DMES group, THP group, EE group, MOM group, or Bn group.
• Compound 4 obtained as above can be isolated and purified by using methods generally used for isolating and purifying organic compounds.
• an elimination reaction proceeds concurrently with the esterification of a free hydroxyl group by reacting Compound 8 with, for example, a sulfonylating agent such as sulfonyl chloride or sulfonic anhydride to produce an E- or Z-olefin derivative.
• a sulfonylating agent such as sulfonyl chloride or sulfonic anhydride
• the isomerization reaction of olefin subsequently proceeds by affecting a base such as DABCO or DBU (1,8-diazabicyclo[5.4.0]undec-7-en) and Compound 9 having a desired steric structure can be obtained.
• Compound 9 obtained as above can be isolated and purified by using methods generally used for isolating and purifying organic compounds.
• Compound 14 can be obtained by reacting Compound 13 with propanal of Compound (C), preferably in the presence of an ammonium salt catalyst such as ethylenediammonium diacetate or pyridinium-p-toluenesulfonate.
• Compound 14 obtained as above is unstable under an acidic condition and can be quickly purified by column chromatography using florisil, or the like.
• Compound 15 can be obtained by epoxidizing Compound 14.
• Compound 15 can be synthesized as follows.
• Compound 15 can be obtained by reacting Compound 14 with peroxide such as tritylperoxide or t-butyl peroxide, preferably in the presence of a base such as butyllithium.
• peroxide such as tritylperoxide or t-butyl peroxide
• a base such as butyllithium
• Compound 15 obtained as above can be isolated and purified by using methods generally used for isolating and purifying organic compounds. In this process, using peroxide capable of stereoselectively epoxidizing Compound 14, the compound represented by the general formula (I) can be stereoselectively synthesized.
• Compound 18 can be obtained by hydrolyzing a cyano group of Compound 16.
• Compound 18 can be synthesized as follows.
• Compounds 17 and 18 can be obtained by developing and purifying in thin-layer chromatography using, as a developing solution, an organic solvent such as ethyl acetate or hexane.
• Compounds 17 and 18 can be also obtained by affecting an acid such as acetic acid, tosylic acid, or hydrochloric acid on Compound 16.
• Compound 17 is transformed into Compound 18 by reacting it with ammonia water or the like.
• Compound 18 obtained as above can be isolated and purified by using methods generally used for isolating and purifying organic compounds.
• the pharmaceutical agent containing the compound of the present invention as an active ingredient can be orally or parenterally administered.
• dosage forms include: oral agents such as powders, granules, tablets, capsules, pills, and solvents; and parenteral agents such as injections, suppositories, percutaneous absorbents, and inhalants.
• the effective amount of the compound can be mixed with, if necessary, a pharmaceutical additive such as an excipient, a binder, a wetting agent, a disintegrant, or a lubricant suitable for the dosage form, and the whole can be subjected to any processing to produce a pharmaceutical preparation.
• a THF solution (15 ml) of tert-butyldimethyl phosphonoacetate (1.257 g; 4.94 mmol) is added to a THF solution (5 ml) of sodium hydride (155.2 mg; 3.88 mmol) at 0° C., and the whole is stirred at room temperature for 0.5 hours.
• a THF solution (5 ml) of Aldehyde 6 (503.9 mg; 1.97 mmol) is then added thereto at 0° C. and the whole is stirred at room temperature for 0.5 hours. After stirring, the resultant solution is quenched using a buffer solution (15 ml) and the organic compound is extracted three times with ethyl acetate, followed by drying over anhydrous magnesium sulfate.
• HMPA 1.6 ml
• a 1.53M butyllithium-hexane solution 2.2 ml; 3.37 mmol
• a THF solution (6 ml) of Ester 7 (665.7 mg; 1.88 mmol) is then added thereto at ⁇ 78° C. and the whole is stirred for 1.5 hours.
• acetaldehyde (2 ml; 35.8 mmol) is added there to at ⁇ 78° C. and the whole is stirred for 3 hours.
• the resultant solution is quenched using a buffer solution (50 ml) and the organic compound is extracted three times with ethyl acetate, followed by the wash of the organic layer in a saturated saline solution and drying over anhydrous magnesium sulfate. Anhydrous magnesium sulfate is filtered and the solvent is distilled off under reduced pressure.
• DABCO (5.67 g; 50.65 mmol) is added to a methanol solution (50 ml) of the resultant mesylate and the whole is refluxed at 100° C. for 120 hours. After stirring, the resultant solution is quenched using a buffer solution (50 ml) and the organic compound is extracted three times with ethyl acetate, followed by the wash of the organic layer in a saturated saline solution and drying over anhydrous magnesium sulfate.
• the activity of the compound of the present invention was measured according to the following method.
• SH-SY5Y cells of human neuroblastoma were cultured in DMEM medium (Dulbecco's modified Eagle medium) (containing 5% fetal bovine serum).
• Compound 1 of the present invention in a series of dilutions was added thereto and cultured at 37° C. under a 5% carbon dioxide atmosphere for 48 hours, followed by adding a MTT (3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyl tetrazoliumbromide) reagent and further culturing for 2 to 4 hours. Absorbance at 570 nm was then measured to calculate the survival ratio.
• Compound 1 of the present invention had a concentration of 0.4 ⁇ g/ml at a 50% growth-inhibiting concentration.
• Compound 1 of the present invention is effective as an antitumor agent.
• a novel compound of the present invention has antitumor activity, and is excellent as an antitumor agent.

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• Organic Chemistry (AREA)
• Veterinary Medicine (AREA)
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• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Epoxy Compounds (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)

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• 2003
  • 2003-06-06 US US10/516,743 patent/US7612213B2/en not_active Ceased
  • 2003-06-06 WO PCT/JP2003/007189 patent/WO2003104238A1/ja active Application Filing
  • 2003-06-06 US US13/092,127 patent/USRE43038E1/en not_active Expired - Fee Related
  • 2003-06-09 JP JP2003164126A patent/JP4523761B2/ja not_active Expired - Fee Related

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