WO2012173447A2 - 1,3-다이옥소인덴 유도체, 이의 약학적으로 허용되는 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 항바이러스용 약학적 조성물 - Google Patents
1,3-다이옥소인덴 유도체, 이의 약학적으로 허용되는 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 항바이러스용 약학적 조성물 Download PDFInfo
- Publication number
- WO2012173447A2 WO2012173447A2 PCT/KR2012/004804 KR2012004804W WO2012173447A2 WO 2012173447 A2 WO2012173447 A2 WO 2012173447A2 KR 2012004804 W KR2012004804 W KR 2012004804W WO 2012173447 A2 WO2012173447 A2 WO 2012173447A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- dioxo
- dihydro
- inden
- isopropyl
- isopropylphenyl
- Prior art date
Links
Classifications
-
- 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
- A61K31/12—Ketones
- A61K31/122—Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/657—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings
- C07C49/665—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61K31/04—Nitro compounds
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/45—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by at least one doubly—bound oxygen atom, not being part of a —CHO group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/20—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/22—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/30—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
- C07C233/32—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/30—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
- C07C233/33—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/41—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/42—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
- C07C233/43—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/57—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C233/61—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/76—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C247/00—Compounds containing azido groups
- C07C247/14—Compounds containing azido groups with azido groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/12—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/24—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
- C07C271/42—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/44—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/62—Compounds containing any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylcarbamates
- C07C271/64—Y being a hydrogen or a carbon atom, e.g. benzoylcarbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/26—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/64—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups singly-bound to oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/22—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and doubly-bound oxygen atoms bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/703—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups
- C07C49/747—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/753—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/753—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
- C07C49/755—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups a keto group being part of a condensed ring system with two or three rings, at least one ring being a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/12—Acetic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/12—Acetic acid esters
- C07C69/16—Acetic acid esters of dihydroxylic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/12—Acetic acid esters
- C07C69/18—Acetic acid esters of trihydroxylic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
- C07C69/28—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with dihydroxylic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/533—Monocarboxylic acid esters having only one carbon-to-carbon double bond
- C07C69/54—Acrylic acid esters; Methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/612—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a six-membered aromatic ring in the acid moiety
- C07C69/618—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a six-membered aromatic ring in the acid moiety having unsaturation outside the six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/62—Halogen-containing esters
- C07C69/63—Halogen-containing esters of saturated acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/734—Ethers
- C07C69/736—Ethers the hydroxy group of the ester being etherified with a hydroxy compound having the hydroxy group bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/738—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C07C69/78—Benzoic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/65—One oxygen atom attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Definitions
- the present invention relates to a 1,3 'dioxoindene derivative, a pharmaceutically acceptable salt thereof or an optical isomer thereof, a preparation method thereof and an antiviral pharmaceutical composition containing the same as an active ingredient.
- Picornavirus is a positive single stranded RNA virus of 7.2-8.5 Kb, a very small spherical virus of about 22-30 nm, the most undiscovered and the oldest known virus.
- viruses belonging to the Picornavirus family include rhinoviruses and polioviruses, Coxsackie virus A, coxsackievirus B, echoviruses, and hepatitis A viruses. It includes an enterovirus (enterovirus) and the like.
- the RA virus picornavirus
- the RA virus picornavirus
- polio paralysis, acute hemorrhagic conjunctivitis, viral meningitis, hand and foot disease, bullous disease, hepatitis A, myositis, myocarditis, ⁇ enteritis, diabetes, epidemic myalgia, encephalitis, cold, herpes stomatitis
- It is a virus that causes various diseases such as respiratory diseases, digestive diseases, circulatory diseases, and skin diseases such as foot and mouth disease.
- Most of the drugs under development are uncoating inhibitors.
- Viruses belonging to the Picornavirus family cause a variety of diseases, such as the above-mentioned respiratory diseases, which cause health, social and economic problems. Picornaviruses form the mainstay of the scalp virus, and are very stable and not easy to disinfect, constantly causing associated viral diseases.
- Human rhinovirus (hRV) is known to be the most common asthma exacerbation factor, and human rhinoviruses are also known to be present in the bronchial tissue of a large number of stable asthmatic patients. Bronchomucosal biopsy samples were obtained from asthma patients and non-asthmatic patients, respectively. The incidence of human rhinoviruses in the lower respiratory tract tissues was significantly higher in the asthma group than in the asthma group. There is also a report that correlates with clinical severity.
- Rhinoviruses are the main cause of colds, and enteroviruses cause many diseases such as meningitis and respiratory infections.
- efforts to vaccinate worldwide have curbed polio-induced polio. It is still present in Niger, Nigeria, Egypt, India, Pakistan and Afghanistan.
- Hepatitis A has also been controlled to some extent by a vaccine against hepatitis A virus.
- vaccines against coxsackieviruses, echoviruses and rhinoviruses have not yet been developed.
- coxsackievirus B is known to cause myocarditis, an idiopathic dilated cardiomyopathy that requires severe heart transplantation.
- Enviroxime derivatives have been studied as promising candidates with broad anti-entrovirus (entervirus) and anti-rhinovirus activity. Enviroxime interferes with the synthesis of plus-stranded RNA by binding to viral protein 3A, which is required for the formation of RNA intermediates during virus regeneration (Heinz BA and Vance LM: J Virol, 1995, 69 (7), 4189-97). .
- Protease inhibitor AG 7088 was studied based on knowledge of the sophisticated structure and function of viral protease 2C. In cell cultures in the nanomolar concentration range, AG 7088 has been shown to be effective against 48 rhinovirus types and coxsackieviruses A21, B3, enterovirus 70 and echovirus 11 (Pattick AK et al .: Antimicrobila Agents Chemother, 1999, 43 (10), 2444-50).
- WIN substance As the molecular structure of the viral capsid became clear, prerequisites for the critical design of the capsid blocker "WIN substance" were studied (Diana GD: Curr Med Chem 2003, 2, 1-12). They inhibit the adsorption and / or exfoliation of rhinoviruses and enteroviruses. Some of the WIN substances have a highly specific effect only on individual genera or virus types of picornaviruses. Other derivatives inhibit the replication of both rhinoviruses and enteroviruses. Arildone, disoxar i 1 and pirodavir belong to the WIN material, for example. These compounds showed very good antiviral effects in cell culture.
- pleconariil is potentially effective against a wide range of viral diseases, from the common cold to viral meningitis or myocarditis. Resistance was observed for rhinoviruses, enterovirus 71 and coxsackievirus B3 (Ledford RM et al .: J Virol 2004, 78 (7), 3663-74; Groarke JM et al .: J Infect Dis 1999, 179 (6), 1538-41). However, the proven therapeutic effect has not been sufficient to name Fleconaril (Picovir, Viropharma, USA) as an agent for treating rhinovirus infection in the United States. In March 2002, the corresponding application was rejected by the Food and Drug Administration (FDA) because side effects were observed and treatment success was too low.
- FDA Food and Drug Administration
- BTA-798 compounds which are more active than flaconanyl in in vitro and in vivo antiviral efficacy evaluations with rhinoviruses, are currently in clinical studies (Ryan, J. et al. Antiviral Res [18th Intl Conf Antiviral Res (April 11-14, Barcelona) 2005] 2005, 65 (3): Abst LB-11).
- no antiviral drugs approved for the treatment of enteroviruses or rhinoviruses have yet been developed.
- the present inventors have studied new antiviral compounds against picornaviruses including coxsackievirus, enterovirus, echovirus, poliovirus, rhinovirus, and the like. Synthesis was confirmed that the derivative has excellent antiviral activity against picornaviruses such as coxsackievirus, enterovirus, echovirus, poliovirus, rhinovirus and the like, and completed the present invention.
- An object of the present invention is to provide a 1, 3-dioxoindene derivative or a pharmaceutically acceptable salt thereof.
- Another object of the present invention is to provide a method for preparing the 1,3-dioxoindene derivative or a pharmaceutically acceptable salt thereof.
- Another object of the present invention to provide a pharmaceutical composition for the prevention or treatment of viral diseases containing the 1,3-dioxoindene derivative or a pharmaceutically acceptable salt thereof as an active ingredient.
- the present invention provides a 1,3-dioxoindene derivative represented by the following formula (1), a pharmaceutically acceptable salt thereof or an optical isomer thereof.
- a 1 , A 2 , A 3 , A 4 , D 1 , D 2 , D 3 , D 4 , Z 1 , Z 2 , Z 3 , X, Y, E and G are as described herein.) '
- the present invention provides a method for preparing the 1, 3-dioxoindene derivatives, pharmaceutically acceptable salts thereof or optical isomers thereof.
- the present invention provides a pharmaceutical composition for preventing or treating a viral disease containing the 1,3-dioxoindene derivative, a pharmaceutically acceptable salt thereof, or an optical isomer thereof as an active ingredient.
- the 1,3-dioxoindene derivatives of the general formula (1) according to the present invention are not only low in poliotoxicity but also highly resistant to picornaviruses such as coxsackievirus, enterovirus, echovirus, poliovirus and rhinovirus.
- polio paralysis, acute hemorrhagic conjunctivitis, viral meningitis, hand and foot disease, bullous disease, hepatitis A, myositis, myocarditis, pancreatitis, diabetes, epidemic myalgia, encephalitis, cold, herpes stomatitis, It can be usefully used as a pharmaceutical composition for the prevention or treatment of viral diseases such as foot and mouth disease, asthma, chronic obstructive pulmonary disease, pneumonia, sinusitis or otitis media.
- viral diseases such as foot and mouth disease, asthma, chronic obstructive pulmonary disease, pneumonia, sinusitis or otitis media.
- the present invention is 1,3-dioxoindene represented by the following formula (1)
- the ring formed by linking at least two substituents may comprise one or more hetero atoms, wherein the hetero atoms are N, 0 or S;
- any one selected from the group consisting of NR3 ⁇ 4 3 , or at least two substituents adjacent to each other among the D 1 , D 2 , D 3, and D 4 may together form a ring, wherein the D 1 , D 2 , D A ring formed by linking at least two substituents adjacent to each other of 3 and D 4 may include one or more hetero atoms, wherein the hetero atoms are N, 0 or S;
- R 1 , R 2 and R 3 are each independently hydrogen, unsubstituted or phenyl ⁇ straight or branched chain alkyl of substituted d Co, alkoxy, unsubstituted or phenyl substituted d do or straight chained alkenyl, C 3 to C 7 cycloalkyl or unsubstituted or substituted with phenyl ( 6 to ( 12 ) aryl;
- X and ⁇ are each independently hydrogen, oxygen, hydrospec or sulfur;
- Z 1 , Z 2 and Z 3 are carbon or nitrogen
- n is an integer from 1 to 10;
- a 1 , A 2 , A 3 and A 4 are independently or optionally selected from the group consisting of halogen, linear or branched alkyl of Crdo, -NR 2 , -NI ⁇ XR 2 , or A 1 , At least two substituents adjacent to each other of A 2 , A 3 and A 4 are . May form a ring together, wherein the ring formed by connecting at least two substituents adjacent to each other among the D 1 , D 2 , D 3, and D 4 may include one or more hetero atoms, and the hetero atoms N, 0 or S; Of
- R 1 , R 2 and R 3 are each independently hydrogen or unsubstituted or substituted with Cphenyl C 9 straight or branched chain alkyl, unsubstituted or phenyl substituted with straight or branched chain alkenyl (: 5 Or (: 6 to (: 10 ) aryl;
- X and ⁇ are each independently oxygen or hydroxy
- Z 1 , Z 2 and Z 3 are carbon
- n is an integer from 1 to 5;
- 'I a single or double bond. More preferably,
- a 1 , A 2 , A 3 and A 4 are independently or optionally any one selected from the group consisting of H, halogen and —NR 2 ; ,
- G is -OH, -NR C)) ⁇ or N ⁇ OXOOR 2 ;
- D 1 , D 2 , D 3 and D 4 are independently or optionally selected from the group consisting of halogen, straight or branched chain alkyl of d-do and -NR C)) ⁇ ;
- E is H, -OH, -OR 1 , -OR 1 , -OCCOX 1 or -0> 0) 2 ;
- R 1 , R 2 and R 3 are each independently hydrogen or unsubstituted or straight chained or branched alkyl of d-Cs substituted with phenyl, d-C 4 straight or branched chain alkenyl or C 6 substituted with unsubstituted or phenyl; Aryl of ⁇ C 10 ;
- X and Y are oxygen
- Z 1 , Z 2 and Z 3 are carbon;
- n is an integer of 1 to 3; ''
- a 1 , A 2 , A 3 and A 4 are independently or optionally any one selected from the group consisting of -H and -NR 2 ;
- G is -NR CR 2 ; '
- D 1 , D 2 , D 3 and D 4 are d-C 10 straight or branched alkyl
- E is-(XCO 1 ;
- R 1 , R 2 and R 3 are each independently hydrogen or d-C 7 straight or branched alkyl; X and Y are oxygen; zz 2 and z 3 are carbon;
- n is an integer of 1 to 3;
- Examples of the 1,3-dioxoindene derivative represented by Chemical Formula 1 according to the present invention are as follows.
- 1,3-dioxoindene derivative represented by the formula (1) of the present invention can be used in the form of a pharmaceutically acceptable salt, pharmaceutically acceptable salts
- Acid addition salts formed by free acid are useful.
- the expression pharmaceutically acceptable salt is a concentration that has a relatively nontoxic and harmless effect on the patient and that any side effects due to the salt do not degrade the beneficial efficacy of the base compound of formula 1, or Means inorganic addition salts.
- These salts can use inorganic and organic acids as free acids, hydrochloric acid, bromate nitrate, sulfuric acid, perchlorate, hydrochloric acid, and phosphoric acid.
- Shiyugigi acid acid is citric acid, acidic acid, lactic acid, maleic acid, fufumarine acid, near-glucoconic acid, me 3 ⁇ 4 F tan Ll Sul ⁇ l foni acid l , Gly; Acid L, succinate , Ethanesulfonic acid, 4-luluenesulfonic acid, salicylic acid, citric acid, benzoic acid or malonic acid can be used.
- these salts include alkali metal salts (sodium salts, potassium salts, etc.), alkaline earth metal salts (such as chame salts, magnesium salts, and the like).
- alkali metal salts sodium salts, potassium salts, etc.
- alkaline earth metal salts such as chame salts, magnesium salts, and the like.
- acid addition salt acetate, aspartate, benzate, benzyl silicate, bicarbonate / carbonate, bisulfate / sulphate, borate
- the acid addition salt ⁇ silver according to the present invention is a conventional method, for example, the derivative of formula 1 is an organic solvent, for example methanol ethanol, acetone, methylene chloride, acetonitrile. 3 ⁇ 4
- the acid can be prepared by distillation under reduced pressure, followed by -g- drying -7 or crystallization under a pre-solvent.
- Alkali metal salts or alkaline earth metal salts dissolve the compound in excess alkali metal hydroxide or alkaline earth metal hydroxide solution and incur Filtrate and evaporate and dry the filtrate.
- the metal salt it is pharmaceutically suitable to prepare sodium, potassium, or chamois salt.
- Silver salts are also obtained by reacting alkali or alkaline earth metal salts with a suitable negative salt (eg silver nitrate).
- the present invention includes not only the phenyl derivative of Formula 1 and pharmaceutically acceptable salts thereof, but also possible solvates, hydrates, isomers, and the like, which may be prepared therefrom. As shown,
- It provides a process for preparing a 1,3-dioxoindene derivative according to the present invention comprising the step of acylating or alkylating a compound of formula 2 in a solvent with a base to obtain a compound of formula la (step 1).
- the compound of Formula la is a derivative of Formula 1, a pharmaceutically acceptable salt thereof, or an optical isomer thereof,
- a 1 , A 2 , A 3 , A 4 , D 1 , D 2 , D 3 , D 4 , Z 1 , Z 2 and Z 3 are the same as defined in Chemical Formula 1,
- the solvent of Scheme 1 is diisopropyl ether, diethyl ether, dioxane, tetrahydrofuran (THF), dimethylformamide (DMF), dimethylacetamide (DMA), dimethyl sulfoxide (DMS0), methylene chloride (MC), chlorobenzene, toluene, benzene and the like can be used.
- the base may be any one selected from the group consisting of pyridine (PPTs), 4'dimethylaminopyridine, trimethylamine and ethylamine.
- PPTs pyridine
- 4'dimethylaminopyridine 4'dimethylaminopyridine
- trimethylamine trimethylamine
- ethylamine 4'dimethylaminopyridine
- Thionyl chlora is reacted with a compound of Formula 2 in a reaction base and a solvent . Reacting with thionyl chloride or oxalic chloride and then reacting with ammonia to obtain a compound of formula 3 (step 1); And
- step 2 Acylating the compound of Formula 3 prepared in Step 1 under a base and a solvent Or alkylation to obtain a compound of formula lb (step 2); provides a method for producing a 1,3-dioxoindene derivative of the present invention comprising a.
- the compound of Formula lb is a derivative of Formula 1, a pharmaceutically acceptable salt thereof, or an optical isomer thereof,
- a 1 , A 2 , A 3 , A 4 , D 1 , D 2 , D 3 , D 4 , Z 1 , Z 2 and Z 3 are the same as defined in Chemical Formula 1,
- Step 1 and Step 2 of Scheme 2 are independently or optionally equal to A 1 , A 2 , A 3 , A 4 , D 1 , D 2 , D 3 or D 4 .
- the solvent of Step 1 and Step 2 of Scheme 2 is diisopropyl ether, ' diethyl ether, dioxane, tetrahydrofuran (THF), dimethylformamide (DMF), dimethylacetamide Any one selected from the group consisting of (DMA), dimethyl sulfoxide (DMS0), methylene chloride (MC), chlorobenzene, toluene and benzene can be used.
- the base in the reaction may be used pyridine (PPTs), trimethylamine, ethylamine and triphosphine.
- PPTs pyridine
- the present invention provides a pharmaceutical composition for the prevention or treatment of a viral disease containing a 1,3-dioxoindene derivative represented by the formula (1), a pharmaceutically acceptable salt thereof or an optical isomer thereof as an active ingredient. do.
- the viral disease is a disease caused by picornavirus including coxsackievirus, enterovirus, poliovirus, rhinovirus and the like.
- the viral diseases include polio, paralysis, acute hemorrhagic conjunctivitis, viral meningitis, hand and foot disease, bullous disease, hepatitis A, myositis, myocarditis, pancreatitis, epidemic myalgia, encephalitis, cold, herpes stomatitis, foot and mouth disease, etc. Can be mentioned.
- the 1,3-dioxoindene derivative of Formula 1 according to the present invention is not only low in cytotoxicity, but also highly antiviral to picornaviruses such as coxsackievirus, enterovirus, ecovirus, poliovirus, rhinovirus and the like.
- Active Active, polio, paralysis, acute hemorrhagic conjunctivitis, viral meningitis, hand and foot disease, bullous disease, hepatitis A, myositis, myocarditis, pancreatitis, diabetes, epidemic myalgia encephalitis, cold, herpes stomatitis, foot and mouth disease, asthma, It can be usefully used as a pharmaceutical composition for the prevention or treatment of viral diseases such as chronic obstructive pulmonary disease, pneumonia, sinusitis or otitis media.
- viral diseases such as chronic obstructive pulmonary disease, pneumonia, sinusitis or otitis media.
- the compounds of the present invention may be administered in various dosage forms, oral and parenteral, for clinical administration, and when formulated, diluents or excipients such as fillers, extenders, binders, wetting agents, disintegrants, surfactants, etc., which are commonly used, may be used. Are manufactured.
- Solid form preparations for oral administration include tablets, patients, powders, granules, capsules, troches, and the like, which form at least one excipient such as starch, calcium carbonate, water Prepared with a mixture of sucrose, lactose or gelatin. In addition to simple excipients, lubricants such as magnesium styrate talc are also used.
- Liquid preparations for oral administration include suspensions, liquid solutions, emulsions, or syrups.In addition to commonly used simple diluents such as water and liquid paraffin, various excipients such as wetting agents, sweeteners, fragrances, and preservatives can be used. May be included.
- Formulations for parenteral administration include sterile aqueous solutions, non-aqueous solvents, suspensions, emulsions; Lyophilized preparations, suppositories, and the like.
- non-aqueous solvent and the suspension solvent propylene glycol, polyethylene glycol, vegetable oil such as olive oil, injectable ester such as ethyl oleate, and the like can be used.
- a suppository base witepsol, macrogol, tween 61, cacao butter, laurin butter, glycerol, gelatin and the like can be used.
- the effective dosage of the compound of the present invention to the human body may vary depending on the age, weight, sex, dosage form, health condition and degree of disease of the patient, and generally about 0.001 to 100 mg / kg / day, preferably Preferably 0.01-35 mg / kg / day. Based on an adult patient weighing 70 kg, typically 0.07-7000 mg / day, preferably 0.72500 mg / day, as determined by the doctor or pharmacist. It may be administered once a day to divided doses at regular time intervals.
- Example 8 4- (2-aceoxy-1,3—dioxo-2, 3-dihydro-IH-inden-2-yl) biphenyl-3-yl acetate
- Example 15 (2-acetoxy-1,3-dioxo-2,3-dihydro-1H-inden-2-yl) -5-tert-butylphenyl acetate
- Example 21 2 (1,3-dioxo-2- (propionyloxy) —2,3-dihydro-IH-inden-2-yl) —5-isopropylphenyl propionate
- Example 24 2 (2-benzyloxy-4-isopropyl-phenyl) -2-hydroxy—indane-1,3-dione 4b, 9b-dihydroxy-7-isopropyl-4b, 9b Hydro-5-oxa-indeno [2, 1- a ] indene- 10-one (0.50 g, 1.68 ⁇ ol) was dissolved in anhydrous DMF (10 ml) and ⁇ potassium carbonate (0.46 g, 3.26 ⁇ ol) Benzyl bromide (0.26 g, 1.51 Pa) was added and stirred at room temperature for 13 hours.
- Example 25 (2-benzyloxy-4-isopropyl-phenyl) -2-mesoxy-indane -1,3'dione 2- (2-benzyloxy-4-isopropyl-phenyl) -2—hydroxy-indane-1,3-dione (0.10 g, 0.25 ⁇ ol) is dissolved in anhydrous DMF (2 ml) and 60% sodium Hydride (0.007 g, 0.31 dl ol) and methyl iodide (0.04 g, 0.28 mmol) were added and stirred at room temperature for 13 hours. The reaction product was concentrated, extracted with dichloromethane, and the concentrated organic layer was purified by column chromatography (ethyl acetate: nucleic acid II 1: 4) to obtain 12 mg (12%) of the title compound. ⁇
- 2-amino-2— (4-isopropyl-2-methoxyphen3 ⁇ 4) -3 ⁇ 4-indene-1,3-dione (200 mg, 0.60 mmol) is dissolved in dichloromethane (10 ml) and cyclopropyl carbonyl Chloride (0.07 mL, 0.77 ⁇ l) and triethylamine (0.27 mL, 1.9 ⁇ l) were added dropwise, followed by stirring overnight at room temperature. The reaction mixture was extracted with dichloromethane and purified by silica gel column chromatography (30% ethyl acetate in nucleic acid). 235 mg (96%) were obtained.
- Example 60 1-ethyl-3- (2,3-dihydrosub 2- (4-isopropyl-2-methoxyphenyl) -1,3- Dioxo-1H—Inden-2-yl) urea.
- the reaction mixture was concentrated and dissolved again in THF (20 mL), and then added hydroxylamine hydrochloride (0.28 g, 4.04 mmol) and triethylamine (0.56 mL, 4.04 mL iol) were stirred at room temperature for 2 hours.
- Example 71 2 (2-aceoxy-1,3—dioxo-2,3-dihydro—IH-inden-2 days) -6—methylpyridin-3-yl acetate
- the target product was synthesized.
- the desired product was synthesized in a similar manner as in Example 24.
- the desired product was synthesized in a similar manner as in Example 24.
- the desired product was synthesized in a similar manner as in Example 24.
- 3 ⁇ 4_ ⁇ (300MHz, CDCI 3 ) ⁇ 2.02 (s, 3H, NAc) 2.20 (s, 3H, CH 3 ) 2.22 (s, 3H, (3 ⁇ 4) ⁇ 6.11 (s, 1H, ArH) 7.03 (s, 1H , ArH) 7.99-8.02 (m, 2H, ArH) 8.13-8.16 (m, 2H, ArH).
- Ni (3,4-dimethylphenyl) propionamide (500 mg, 2.82 mmoles) and ninhydrin (500 mg, 2.82 mmoles) were dissolved in conc.H 2 SO 4 (10 ml) and stirred at room temperature. After 1.5 hours, the reaction was completed by stirring with ice (150 g) slowly. The reaction was extracted with ethyl acetate and water, the organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure. Silica gel column chromatography (30% ethyl aceate in 430 mg (45%) of a yellow solid compound was separated and purified.
- N- (3-ethylphenyl) acetamide (500 mg, 3.06 mmoles) and ninhydrin (546 mg, 3.06 ⁇ oles) were dissolved in conc.H 2 SO 4 (10 ml) and stirred at room temperature. After 3 hours, the reaction was completed by stirring with ice (150 g) slowly. The reaction was extracted with ethyl acetate and water, the organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure. Silica gel column chromatography (30% ethyl acetate in hexanes) was purified by separation to give 90 mg (9%) of the compound.
- N- (3,4-dimethylphenyl) butyramide (1.00 g, 5.61 ⁇ oles) and ninhydrin (1.07 g, 5.61 ⁇ oles) are dissolved in conc.H 2 S0 4 (15 ml) and stirred at room temperature It was. After 5 hours, the reaction was completed by stirring with ice (150 g) slowly. The reaction was extracted with ethyl acetate and water, the organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure. Separation and purification by silica gel column chromatography (30% ethyl aceate in hexanes) gave 1.10 g (56%) of a yellow solid compound.
- N- (3,4-dimethylphenyl) isobutyramide L00 g, 5.61 ⁇ oles) and ninhydrin (1.07 g, 5.61 ⁇ oles) were dissolved in cone.3 ⁇ 4SO 4 (15 ml) and stirred at room temperature. After 5 hours, the reaction was completed by stirring with ice (200 g) slowly. The reaction was extracted with ethyl acetate and water, the organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure. Separation and purification by silica gel column chromatography (30% ethyl aceate in hexanes) gave 1.85 g (94%) of a yellow solid compound.
- N- (2,2-dihydroxy-7-nitro— 1, 3-dioxo-2, 3-dihydro-1H-indene-4—yl) acetamide (0.20 g, 0.71 oles) and N- (3, 4-dimethylphenyl) isobutyramide (136 mg, 0.71 dl oles) was dissolved in conc.3 ⁇ 4SO 4 (5 ml) and stirred at room temperature for 3 hours. The reaction was extracted with ethyl acetate and ice water, the organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure. Silica gel column chromatography (30% ethyl aceate in hexanes) was purified by separation to give 30 mg (10%) of the compound.
- Example 96 2 (2-Acetamido—4-amino-1,3—dioxium 2,3′dihydro-1H-inden-2-yl) -5-isopropylphenyl butyl carbonate 2- ( 2-acetamido-4-amino-1,3-dioxo-2,3-dihydro-1H-inden-2-2-yl) -5-isopropylphenyl butyl carbonate
- Example 102 Ethyl Acetyl (2- (2-Hydroxy-4-isopropylphenyl) -1,3-dioxo-2,3-dihydro-1H-indenyl 2-yl) carbamate ⁇ ⁇ chloro -4b-hydroxy-7-isopropyl- 1-nitro-4bH-benzo [d] indeno [1,2-b] furan-10 (9bH)-(0.70 g, 2.07 mmol) was dissolved in anhydrous THF ( 15 ml), ethyl chloroformate (0.32 g, 3.11 mmol) and trimethylamine (0.25 g, 2.48 dl) were added and stirred for 4 hours.
- Example 104 2 (3-methoxyphenyl) —2H-indene—1,3-dione
- Example 106 N- (2- (2-hydroxy-1,3-dioxo-2,3-dihydro-lH-inden-2-yl) ⁇ 4,5-dimethoxyphenyl) isobutyramide Nininhydrin (1.00 g, 5.6 ⁇ l ol) was dissolved in conc.H 2 S0 4 (10 ml) and N- (3,4-dimethoxyphenyl) isobutyramide (1.25 g, 5.62 mmol) was added to 0 o was added at C and allowed to react at room temperature for 30 minutes.
- cells were HeLa (human cervical malignant tumor cells), MRC-5 (human embryonic lung cells), RD (human embryonic muscle cells), and standard drugs were ribavirin (Ribavirin, Riv), and flaconaril. (Pleconari 1, pleco), BTA-798 (BTA) was used.
- samples are dissolved in 100% dimethyl sulfoxide (DMS0) at 10-40 mg / ml, and samples dissolved in water are dissolved in PBS (-) solution and stored at -20 ° C. The concentration of dimethyl sulfoxide in the wells was not to exceed 0.5% or higher.
- Drug screening was conducted using the £ PATIC effect (CPE) inhibition method during virus induction. / ' Proliferate the appropriate cells according to the virus in 96-well plates, and then dilute the virus diluted with DME (DME / 2 FBS) containing 2% FBS or MEM (MEM / 2% FBS) containing 2% FBS. Each well was inoculated at 100 ccID 50 (50% cell culture inhibition) and then adsorbed at 33 ° C. or 37 0 C for 30 minutes to 1 hour and then culture was removed. Replicate diluted drugs at each concentration, add 100 ⁇ to each well and incubate at 33 ° C
- CPE £ PATIC effect
- Viruses other than HRV were incubated for 2 to 3 days in a 37 ° C C0 2 incubator, or cells were dosed with a double dose of 50 ⁇ followed by 50 ⁇ virus solution and then cultured for 2-3 days without removal of the culture solution. .
- the concentration of the drug that survived 50% of cells by MTT was determined as EC 50 (50% effective concentration).
- CPE measurements were determined by FDA (Fluorescein diacetate).
- the culture was added to the cells without the addition of the virus at the time of inoculation, and then treated in the same manner as the cells inoculated with the mock-infected virus. That is, after one hour of incubation, the medium was removed and the diluted drug was added once more to the culture.
- the survival rate is 100% is not toxic, if the survival rate is o% is the most toxic.
- the concentration of the drug capable of killing 50% of the cells is expressed as CC 50 , which means that the higher the value, the less toxic.
- antiviral effect can be calculated through the following equation (2).
- Anti " by I human effect drug / virus)-virus control) 100%
- CC 50 concentrations that are cytotoxic to compounds EC 50 concentration showing activity against several viruses belonging to the Picornavirus
- the 1,3-dioxoindene derivative according to the present invention exhibits a high CC 50 concentration, and thus it can be seen that the cytotoxicity is low.
- the 1,3-dioxoindene derivative according to the present invention exhibits an EC 50 concentration of 0.01 / g / mL or less against coxsackieviruses, polioviruses, rhinoviruses, and enteroviruses, and has high antiviral activity. Appeared.
- the 1,3 ⁇ dioxoindene derivative represented by the formula (1) according to the present invention exhibits low cytotoxicity and high antiviral activity against various viruses, such as coxsackievirus, enterovirus, ecovirus, poliovirus and It may be useful as a pharmaceutical composition for the prevention or treatment of diseases caused by picornavirus to which rhinovirus belongs.
- Anti-picornavirus efficacy screening was performed using a multicycle CPE reduction assay.
- the antiviral activity of the compounds is based on 3 ⁇ 4 Che (4,5-dimethylthiazol-2-yl) -5 ⁇ (3-carboxymethyphenyl) -2 ⁇ (4-sulfophenyl) -2H-tetrazolium]. It was initially determined by one CPE reduction assay.
- each virus was transferred to cells proliferated for fusion in 96well well plates. Each well inoculum was inoculated to 100 CCID 50 (50 cell culture inhibitory amount). After 2 hours of adsorption at 37 0 C, the virus was removed and stepwise diluted compounds were added. Cultured cells were further incubated for 3 days at 37 ° C until induced but untreated control virus (VC) was determined to be complete CPE. Subsequently, the mediator was removed and 90 ⁇ cultured cell mediator and 10 ⁇ MTS-phenazine methosulfate (Promega, Leiden, The Netherlands) were added to each well. After 2 hours of incubation at 37 ° C, the microplate reader was used to measure the 0D (optical density) value of each cell at 498 nm.
- CCID 50 50 cell culture inhibitory amount
- The% CPE value for antiviral efficacy evaluation was calculated by the following equation.
- PE value for cytotoxicity measurement of the drug was calculated by the following equation (4).
- OD (CC) is 0D of the background solution culture cells which are not virus-induced and do not undergo compound treatment
- OD (VC) was induced in virus-induced and untreated compounds in control cultured cells.
- 0D (virus + compound) is 0D of cultured cells infected with the virus treated with the concentrated compound
- 0D (Compound) is 0D of cultured cells treated with concentrated compound only
- OD (Blank) is 0D of the wells to which only the culture was added.
- the effective concentration (EC 50 ) is the concentration of the drug that allows 5OT cells to survive by the CPE of the induced virus
- the cytotoxicity concentration (CC 50 ) is the concentration of the drug at which the compound killed 50% of the cells. logarithmic interpolat ion). CC 50 and EC 50 for various viruses are shown in Table 5 for some example compounds.
- the 1,3-dioxoindene derivative according to the present invention showed an EC 50 value of 3.3 ⁇ or less with respect to the Entero 71 virus, and particularly in Example 36, a low value of 0.0067 ⁇ or less.
- the 1,3-dioxoindene derivative according to the present invention is directed against Echo 9 and Echo 11 viruses.
- the low EC 50 value indicates excellent antiviral activity.
- the 1,3-dioxoindene derivative according to the present invention has an EC 50 value of 20 ⁇ or less for the Polaro 1, 2, 3 virus. , Especially of Example 36 If it can be seen to represent a ", excellent anti-viral activity by showing a low EC 50 value of less than or equal to 0.01 ⁇ .
- the 1,3-dioxoindene derivative according to the present invention is rhinoviruses, for example 2, 9, 15, 29, 39, 41, 45, 59, 63, 85, 89, 14, 42, 70,
- EC 50 was found to be greater than 50 ⁇ against 72 and 86 viruses, in particular Examples.
- the 1,3-dioxoindene derivative according to the present invention is low in cytotoxicity, coxsackievirus, enterovirus,.
- the tablets were prepared by tableting according to the method for preparing tablets in which all of the above components were mixed.
- the capsules were prepared by layering the gelatine capsules according to a conventional method for preparing capsules.
- the solution was filled into a 5 type I ampoule made of clear glass, encapsulated under an upper grid of air by dissolving the glass, and sterilized by autoclaving at 120 0 C for at least 15 minutes to prepare an injection solution.
- the 1,3-diode iindene derivative of Formula 1 according to the present invention not only has low cytotoxicity, but also has very good antiviral activity against tuchnaviruses such as coxsackievirus, enterovirus, ecovirus poliovirus, rhinovirus, etc.
- polio "numbness, acute hemorrhagic conjunctivitis, viral meningitis, hand, foot and mouth disease, the number of artillery, a hepatitis, myositis, myocarditis, pancreatitis, diabetes, epidemic myalgia eu encephalitis, cold, Herpangina, foot-and-mouth disease, asthma , Can be usefully used as a pharmaceutical composition for the prevention or treatment of viral diseases such as chronic obstructive pulmonary disease, pneumonia, sinusitis or otitis media.
- viral diseases such as chronic obstructive pulmonary disease, pneumonia, sinusitis or otitis media.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Neurology (AREA)
- Pulmonology (AREA)
- Oncology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Otolaryngology (AREA)
- Molecular Biology (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Priority Applications (16)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014515763A JP5941142B2 (ja) | 2011-06-16 | 2012-06-18 | 1,3−ジオキソインデン誘導体、その薬学的に許容される塩又は光学異性体、その調製方法及びそれを抗ウイルス活性成分として含有する医薬組成物 |
US14/126,479 US9346749B2 (en) | 2011-06-16 | 2012-06-18 | 1,3-di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient |
EA201490025A EA025384B1 (ru) | 2011-06-16 | 2012-06-18 | Производные 1,3-диоксоиндена, их фармацевтически приемлемая соль, способ их получения и фармацевтическая антивирусная композиция, содержащая их в качестве активного ингредиента |
SI201231664T SI2722322T1 (sl) | 2011-06-16 | 2012-06-18 | 1,3-di-okso-indenski derivat, farmacevtsko sprejemljiva sol ali optični izomer le-tega, postopek njegov priprave in farmacevtski sestavek, ki ga vsebuje kot protivirusno aktivno sestavino |
CA2838680A CA2838680C (en) | 2011-06-16 | 2012-06-18 | 2-phenylindane-1,3-dione derivatives as antiviral agents |
CN201280029665.4A CN103748060B (zh) | 2011-06-16 | 2012-06-18 | 1,3-二氧代茚衍生物、其药学上可接受的盐或光学异构体,其制备方法以及包含其作为抗病毒活性成分的药物组合物 |
MX2013014239A MX355498B (es) | 2011-06-16 | 2012-06-18 | Derivados de 1,3-dioxoindeno, sal farmaceuticamente aceptable de los mismos, metodos de preparacion de los mismos y composicion farmaceutica para el antivirus que contiene el mismo como un ingrediente activo. |
BR112013032273-0A BR112013032273B1 (pt) | 2011-06-16 | 2012-06-18 | Compostos derivados de 1,3-dioxoindeno, seus usos, métodos de preparação dos mesmos e composições farmacêutica |
RU2014101179/04A RU2566761C2 (ru) | 2011-06-16 | 2012-06-18 | Производные 1,3-диоксоиндена, их фармацевтически приемлемая соль, способ их получения и фармацевтическая антивирусная композиция, содержащая их в качестве активного ингредиента |
ES12799827T ES2744982T3 (es) | 2011-06-16 | 2012-06-18 | Derivado de 1,3-di-oxo-indeno, sal farmacéuticamente aceptable o isómero óptico del mismo, método de preparación del mismo, y composición farmacéutica que contiene al mismo, principio activo, antiviral |
AU2012270310A AU2012270310B2 (en) | 2011-06-16 | 2012-06-18 | 1,3-Di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient |
EP12799827.6A EP2722322B8 (en) | 2011-06-16 | 2012-06-18 | 1,3-di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient |
PL12799827T PL2722322T3 (pl) | 2011-06-16 | 2012-06-18 | 1,3-Di-okso-indenowa pochodna, jej farmaceutycznie dopuszczalna sól lub izomer optyczny, sposób jej wytwarzania i kompozycja farmaceutyczna ją zawierająca jako przeciwwirusowy składnik czynny |
EP23218086.9A EP4360710A2 (en) | 2011-06-16 | 2012-06-18 | 1,3-di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient |
EP19179546.7A EP3611158B1 (en) | 2011-06-16 | 2012-06-18 | 1,3-di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient |
US15/098,972 US9833423B2 (en) | 2011-06-16 | 2016-04-14 | 1,3-Di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2011-0058704 | 2011-06-16 | ||
KR20110058704 | 2011-06-16 | ||
KR10-2012-0065023 | 2012-06-18 | ||
KR1020120065023A KR101391745B1 (ko) | 2011-06-16 | 2012-06-18 | 1,3-다이옥소인덴 유도체, 이의 약학적으로 허용되는 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 항바이러스용 약학적 조성물 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/126,479 A-371-Of-International US9346749B2 (en) | 2011-06-16 | 2012-06-18 | 1,3-di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient |
US15/098,972 Continuation US9833423B2 (en) | 2011-06-16 | 2016-04-14 | 1,3-Di-oxo-indene derivative, pharmaceutically acceptable salt or optical isomer thereof, preparation method thereof, and pharmaceutical composition containing same as an antiviral, active ingredient |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2012173447A2 true WO2012173447A2 (ko) | 2012-12-20 |
WO2012173447A3 WO2012173447A3 (ko) | 2013-04-04 |
Family
ID=47357637
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2012/004804 WO2012173447A2 (ko) | 2011-06-16 | 2012-06-18 | 1,3-다이옥소인덴 유도체, 이의 약학적으로 허용되는 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 항바이러스용 약학적 조성물 |
Country Status (16)
Country | Link |
---|---|
US (2) | US9346749B2 (ko) |
EP (3) | EP2722322B8 (ko) |
JP (2) | JP5941142B2 (ko) |
KR (1) | KR101391745B1 (ko) |
CN (1) | CN103748060B (ko) |
AU (1) | AU2012270310B2 (ko) |
BR (1) | BR112013032273B1 (ko) |
CA (1) | CA2838680C (ko) |
EA (1) | EA025384B1 (ko) |
ES (1) | ES2744982T3 (ko) |
MX (1) | MX355498B (ko) |
PL (1) | PL2722322T3 (ko) |
PT (1) | PT2722322T (ko) |
RU (1) | RU2566761C2 (ko) |
SI (1) | SI2722322T1 (ko) |
WO (1) | WO2012173447A2 (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105121433A (zh) * | 2012-12-14 | 2015-12-02 | 韩国化学研究院 | 新型化合物、其药学上可接受的盐或光学异构体、用于制备它们的方法以及包含它们作为有效成分的用于预防或治疗病毒性疾病的药物组合物 |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104557559B (zh) * | 2015-01-14 | 2016-08-17 | 成都中医药大学 | 茚满二酮手性环己烷螺环化合物及其制备方法与用途 |
KR102067858B1 (ko) | 2016-05-24 | 2020-01-17 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 색재 조성물 및 이를 포함하는 수지 조성물 |
EP4139290A1 (en) * | 2020-04-20 | 2023-03-01 | Novartis AG | Antiviral 1,3-di-oxo-indene compounds |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1425295A (en) * | 1974-01-23 | 1976-02-18 | Rizh Politekhn I | Alpha-aminoylidenephthalides and processes for their preparation |
FR2392951A2 (fr) | 1975-02-07 | 1978-12-29 | Creat Lab | Nouveaux derives de la ninhydrine, leurs procedes de preparation et medicaments contenant ces derives |
GB1533388A (en) | 1975-02-07 | 1978-11-22 | Creat | Ninhydrin-phenol condensation products their preparation and use as therapeutic agents |
GB8327598D0 (en) * | 1983-10-14 | 1983-11-16 | Akzo Nv | Pharmacologically active diarylindane-13-diones |
CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
JP2001089455A (ja) | 1999-09-17 | 2001-04-03 | Maruishi Pharmaceutical Co Ltd | 5,10−ジヒドロ−11H−インデノ〔1,2−b〕キノリン−10−オン誘導体 |
DE60013994T2 (de) | 1999-08-30 | 2005-10-06 | Maruishi Pharmaceutical Co.Ltd. | 1,2-Disubstituierte 1,4-Dihydro-4-oxochinolin-Verbindungen |
WO2003082265A2 (en) | 2002-04-02 | 2003-10-09 | Fujisawa Pharmaceutical Co | Pharmaceutical composition for treating or preventing virus infectious diseases |
EP1608369B1 (en) | 2003-03-28 | 2013-06-26 | Novartis Vaccines and Diagnostics, Inc. | Use of organic compounds for immunopotentiation |
WO2008018833A1 (en) * | 2006-08-08 | 2008-02-14 | Agency For Science, Technology And Research | Methods for electrochemical detection/quantification of a nucleic acid |
EP2307440A4 (en) * | 2008-07-01 | 2012-12-19 | Zacharon Pharmaceuticals Inc | HEPARAN SULFATE INHIBITORS |
EP2324820B1 (en) | 2009-11-04 | 2016-03-02 | Inopharm Limited | Stable fluindione composition comprising one or more antioxidant agents |
-
2012
- 2012-06-18 CN CN201280029665.4A patent/CN103748060B/zh active Active
- 2012-06-18 EP EP12799827.6A patent/EP2722322B8/en active Active
- 2012-06-18 KR KR1020120065023A patent/KR101391745B1/ko active IP Right Grant
- 2012-06-18 EP EP19179546.7A patent/EP3611158B1/en active Active
- 2012-06-18 JP JP2014515763A patent/JP5941142B2/ja active Active
- 2012-06-18 US US14/126,479 patent/US9346749B2/en active Active
- 2012-06-18 BR BR112013032273-0A patent/BR112013032273B1/pt active IP Right Grant
- 2012-06-18 EP EP23218086.9A patent/EP4360710A2/en active Pending
- 2012-06-18 WO PCT/KR2012/004804 patent/WO2012173447A2/ko active Application Filing
- 2012-06-18 RU RU2014101179/04A patent/RU2566761C2/ru active
- 2012-06-18 AU AU2012270310A patent/AU2012270310B2/en active Active
- 2012-06-18 MX MX2013014239A patent/MX355498B/es active IP Right Grant
- 2012-06-18 CA CA2838680A patent/CA2838680C/en active Active
- 2012-06-18 PT PT12799827T patent/PT2722322T/pt unknown
- 2012-06-18 ES ES12799827T patent/ES2744982T3/es active Active
- 2012-06-18 SI SI201231664T patent/SI2722322T1/sl unknown
- 2012-06-18 EA EA201490025A patent/EA025384B1/ru not_active IP Right Cessation
- 2012-06-18 PL PL12799827T patent/PL2722322T3/pl unknown
-
2016
- 2016-04-14 US US15/098,972 patent/US9833423B2/en active Active
- 2016-05-18 JP JP2016099511A patent/JP6373297B2/ja active Active
Non-Patent Citations (10)
Title |
---|
DIANA G D, CURR MED CHEM, vol. 2, 2003, pages 1 - 12 |
GROARKE J M ET AL., J INFECT DIS, vol. 179, no. 6, 1999, pages 1538 - 41 |
HEINZ B A; VANCE L M, J VIROL, vol. 69, no. 7, 1995, pages 4189 - 97 |
LEDFORD R M ET AL., J VIROL, vol. 78, no. 7, 2004, pages 3663 - 74 |
MCKINLAY M A ET AL., ANNU REV MICROBIOL, vol. 46, 1992, pages 635 - 54 |
MILLER FD ET AL., ANTIMICROB AGENTS CHEMOTHER, vol. 27, no. 1, 1985, pages 102 - 6 |
PATTICK A K ET AL., ANTIMICROBILA AGENTS CHEMOTHER, vol. 43, no. 10, 1999, pages 2444 - 50 |
PEVEAR D C ET AL., ANTIMICROB AGENTS CHEMOTHER, vol. 43, no. 9, 1999, pages 2109 - 15 |
RYAN, J. ET AL., ANTIVIRAL RES [18TH INTL CONF ANTIVIRAL RES, vol. 65, no. 3, 11 April 2005 (2005-04-11) |
See also references of EP2722322A4 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105121433A (zh) * | 2012-12-14 | 2015-12-02 | 韩国化学研究院 | 新型化合物、其药学上可接受的盐或光学异构体、用于制备它们的方法以及包含它们作为有效成分的用于预防或治疗病毒性疾病的药物组合物 |
CN105121433B (zh) * | 2012-12-14 | 2018-01-23 | 韩国化学研究院 | 抗病毒化合物、其药学上可接受的盐或光学异构体、用于制备它们的方法以及包含它们作为有效成分的用于预防或治疗病毒性疾病的药物组合物 |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101391746B1 (ko) | 인다논 유도체, 이의 약학적으로 허용되는 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 바이러스성 질환의 예방 또는 치료용 약학적 조성물 | |
JP6373297B2 (ja) | 1,3−ジオキソインデン誘導体、その薬学的に許容される塩又は光学異性体、その調製方法及びそれを抗ウイルス活性成分として含有する医薬組成物 | |
KR101630243B1 (ko) | 신규한 화합물, 이의 약학적으로 허용가능한 염 또는 이의 광학 이성질체, 이의 제조방법 및 이를 유효성분으로 함유하는 바이러스성 질환의 예방 또는 치료용 약학적 조성물 | |
ES2974025T3 (es) | Derivado de 1,3-di-oxo-indeno, sal farmacéuticamente aceptable o isómero óptico del mismo, método de preparación del mismo, y composición farmacéutica que contiene al mismo, principio activo, antiviral | |
KR20190041202A (ko) | 항바이러스 화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 바이러스성 질환의 예방 또는 치료용 약학적 조성물 | |
RU2574591C2 (ru) | Производное инданона, его фармацевтически приемлемая соль или энантиомер, способ его получения и содержащая его фармацевтическая композиция для профилактики или лечения вирусного заболевания |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12799827 Country of ref document: EP Kind code of ref document: A2 |
|
WWE | Wipo information: entry into national phase |
Ref document number: MX/A/2013/014239 Country of ref document: MX |
|
ENP | Entry into the national phase |
Ref document number: 2838680 Country of ref document: CA |
|
ENP | Entry into the national phase |
Ref document number: 2014515763 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 14126479 Country of ref document: US |
|
REG | Reference to national code |
Ref country code: BR Ref legal event code: B01A Ref document number: 112013032273 Country of ref document: BR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 201490025 Country of ref document: EA |
|
ENP | Entry into the national phase |
Ref document number: 2012270310 Country of ref document: AU Date of ref document: 20120618 Kind code of ref document: A Ref document number: 2014101179 Country of ref document: RU Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 112013032273 Country of ref document: BR Kind code of ref document: A2 Effective date: 20131216 |