SU1475487A3 - Способ получени производных дифосфоновой кислоты или их натриевых солей - Google Patents
Способ получени производных дифосфоновой кислоты или их натриевых солей Download PDFInfo
- Publication number
- SU1475487A3 SU1475487A3 SU853935742A SU3935742A SU1475487A3 SU 1475487 A3 SU1475487 A3 SU 1475487A3 SU 853935742 A SU853935742 A SU 853935742A SU 3935742 A SU3935742 A SU 3935742A SU 1475487 A3 SU1475487 A3 SU 1475487A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- optionally substituted
- acid
- alkyl
- nmr
- yield
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 5
- XQRLCLUYWUNEEH-UHFFFAOYSA-N diphosphonic acid Chemical class OP(=O)OP(O)=O XQRLCLUYWUNEEH-UHFFFAOYSA-N 0.000 title claims description 6
- 159000000000 sodium salts Chemical class 0.000 title description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
- 208000037147 Hypercalcaemia Diseases 0.000 claims description 5
- 230000000148 hypercalcaemia Effects 0.000 claims description 5
- 208000030915 hypercalcemia disease Diseases 0.000 claims description 5
- 125000006181 4-methyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])C([H])([H])* 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims 1
- 229910014033 C-OH Inorganic materials 0.000 claims 1
- 229910014570 C—OH Inorganic materials 0.000 claims 1
- IUHFWCGCSVTMPG-UHFFFAOYSA-N [C].[C] Chemical class [C].[C] IUHFWCGCSVTMPG-UHFFFAOYSA-N 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- -1 1,2,4-triazole radical Chemical class 0.000 abstract description 11
- 238000002360 preparation method Methods 0.000 abstract description 2
- 150000003839 salts Chemical class 0.000 abstract description 2
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000003277 amino group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 abstract 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical group [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 229930195734 saturated hydrocarbon Natural products 0.000 abstract 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 abstract 1
- 239000011734 sodium Substances 0.000 description 26
- 238000002425 crystallisation Methods 0.000 description 12
- 230000008025 crystallization Effects 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 201000008482 osteoarthritis Diseases 0.000 description 2
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 2
- 150000004492 retinoid derivatives Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 2
- ILUXSIMRASQJIQ-UHFFFAOYSA-N (1-hydroxy-1-phosphono-3-pyridin-2-ylpropyl)phosphonic acid Chemical compound OP(=O)(O)C(P(O)(O)=O)(O)CCC1=CC=CC=N1 ILUXSIMRASQJIQ-UHFFFAOYSA-N 0.000 description 1
- MIOSUYQMFQSETN-UHFFFAOYSA-N (1-hydroxy-1-phosphono-3-pyridin-4-ylpropyl)phosphonic acid Chemical compound OP(=O)(O)C(P(O)(O)=O)(O)CCC1=CC=NC=C1 MIOSUYQMFQSETN-UHFFFAOYSA-N 0.000 description 1
- 125000001359 1,2,3-triazol-4-yl group Chemical group [H]N1N=NC([*])=C1[H] 0.000 description 1
- QFMZQPDHXULLKC-UHFFFAOYSA-N 1,2-bis(diphenylphosphino)ethane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCP(C=1C=CC=CC=1)C1=CC=CC=C1 QFMZQPDHXULLKC-UHFFFAOYSA-N 0.000 description 1
- HQZXWGJQZSXBFQ-UHFFFAOYSA-N 2-(2h-triazol-4-yl)propanoic acid Chemical compound OC(=O)C(C)C=1C=NNN=1 HQZXWGJQZSXBFQ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- AUBVNSHIGBWECH-UHFFFAOYSA-N 3-(1,2,4-triazol-1-yl)butanoic acid Chemical compound OC(=O)CC(C)N1C=NC=N1 AUBVNSHIGBWECH-UHFFFAOYSA-N 0.000 description 1
- KIJGYTNIFKJHJQ-UHFFFAOYSA-N 3-(1,2,4-triazol-1-yl)propanoic acid Chemical compound OC(=O)CCN1C=NC=N1 KIJGYTNIFKJHJQ-UHFFFAOYSA-N 0.000 description 1
- MSTFJGHRCNXOLP-UHFFFAOYSA-N 3-(1-benzylimidazol-2-yl)propanoic acid Chemical compound OC(=O)CCC1=NC=CN1CC1=CC=CC=C1 MSTFJGHRCNXOLP-UHFFFAOYSA-N 0.000 description 1
- LOESLMDNPQYFOG-UHFFFAOYSA-N 3-(1h-imidazol-2-yl)propanoic acid Chemical compound OC(=O)CCC1=NC=CN1 LOESLMDNPQYFOG-UHFFFAOYSA-N 0.000 description 1
- YUEMXJRPUGSFBF-UHFFFAOYSA-N 3-(1h-imidazol-5-yl)propanoic acid;hydrochloride Chemical compound Cl.OC(=O)CCC1=CNC=N1 YUEMXJRPUGSFBF-UHFFFAOYSA-N 0.000 description 1
- WDGXIUUWINKTGP-UHFFFAOYSA-N 3-(3-pyridinyl)propanoic acid Chemical compound OC(=O)CCC1=CC=CN=C1 WDGXIUUWINKTGP-UHFFFAOYSA-N 0.000 description 1
- WSXGQYDHJZKQQB-UHFFFAOYSA-N 3-pyridin-4-ylpropanoic acid Chemical compound OC(=O)CCC1=CC=NC=C1 WSXGQYDHJZKQQB-UHFFFAOYSA-N 0.000 description 1
- NLAOMPHIYUFTPV-UHFFFAOYSA-N 5-(2h-triazol-4-yl)pentanoic acid Chemical compound OC(=O)CCCCC1=CNN=N1 NLAOMPHIYUFTPV-UHFFFAOYSA-N 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- HODREDGUVXRBQL-UHFFFAOYSA-N [1-hydroxy-1-phosphono-3-(1,2,4-triazol-1-yl)butyl]phosphonic acid Chemical compound OP(=O)(O)C(O)(P(O)(O)=O)CC(C)N1C=NC=N1 HODREDGUVXRBQL-UHFFFAOYSA-N 0.000 description 1
- JTHOGGRCTXHEGM-UHFFFAOYSA-N [1-hydroxy-3-(1h-imidazol-2-yl)-1-phosphonopropyl]phosphonic acid Chemical compound OP(=O)(O)C(P(O)(O)=O)(O)CCC1=NC=CN1 JTHOGGRCTXHEGM-UHFFFAOYSA-N 0.000 description 1
- SENMVLWIYCTYJN-UHFFFAOYSA-N [3-(1h-benzimidazol-2-yl)-1-hydroxy-1-phosphonopropyl]phosphonic acid Chemical compound C1=CC=C2NC(CCC(O)(P(O)(O)=O)P(O)(O)=O)=NC2=C1 SENMVLWIYCTYJN-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- GNHQSAUHXKRQMC-UHFFFAOYSA-N benzene;chlorine Chemical compound [Cl].C1=CC=CC=C1 GNHQSAUHXKRQMC-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003412 degenerative effect Effects 0.000 description 1
- XQRLCLUYWUNEEH-UHFFFAOYSA-L diphosphonate(2-) Chemical compound [O-]P(=O)OP([O-])=O XQRLCLUYWUNEEH-UHFFFAOYSA-L 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3839—Polyphosphonic acids
-
- 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
-
- 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
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/58—Pyridine rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
- C07F9/6518—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/653—Five-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Obesity (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Non-Portable Lighting Devices Or Systems Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3428524A DE3428524A1 (de) | 1984-08-02 | 1984-08-02 | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1475487A3 true SU1475487A3 (ru) | 1989-04-23 |
Family
ID=6242211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU853935742A SU1475487A3 (ru) | 1984-08-02 | 1985-08-01 | Способ получени производных дифосфоновой кислоты или их натриевых солей |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US4687767A (enExample) |
| EP (1) | EP0170228B1 (enExample) |
| JP (1) | JPS6143197A (enExample) |
| AT (1) | ATE39489T1 (enExample) |
| AU (1) | AU553419B2 (enExample) |
| CA (1) | CA1264326A (enExample) |
| CS (1) | CS257277B2 (enExample) |
| DD (1) | DD236533A5 (enExample) |
| DE (2) | DE3428524A1 (enExample) |
| DK (1) | DK345285A (enExample) |
| ES (1) | ES8606876A1 (enExample) |
| FI (1) | FI78915C (enExample) |
| GR (1) | GR851881B (enExample) |
| HU (1) | HU196419B (enExample) |
| IL (1) | IL75971A (enExample) |
| SU (1) | SU1475487A3 (enExample) |
| ZA (1) | ZA855760B (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2124019C1 (ru) * | 1992-05-29 | 1998-12-27 | Дзе Проктер энд Гэмбл Фармасьютикалз, Инк. | Тиозамещенные пиридинилбисфосфоновые кислоты или их фармацевтически приемлемые соли или эфиры, фармацевтическая композиция на их основе и способ лечения |
| RU2154647C2 (ru) * | 1993-08-25 | 2000-08-20 | Мерк Энд Ко., Инк. | ЦИКЛИЧЕСКИЕ ФОСФОРСОДЕРЖАЩИЕ СОЕДИНЕНИЯ И СПОСОБ НЕПРЕРЫВНОГО ПОЛУЧЕНИЯ γ-АМИНО-1-ГИДРОКСИАЛКИЛИДЕН-1,1-БИСФОСФОНОВЫХ КИСЛОТ |
| RU2188011C2 (ru) * | 1995-06-05 | 2002-08-27 | Такеда Кемикал Индастриз, Лтд. | Активирующая остеогенез фармацевтическая композиция |
| RU2236415C2 (ru) * | 2000-02-01 | 2004-09-20 | Дзе Проктер Энд Гэмбл Компани | Способ селективного получения полупентагидрата и моногидрата натриевой соли 3-пиридил -1-гидроксиэтилиден-1,1-бисфосфоновой кислоты и фармацевтическая композиция на их основе |
| RU2319706C2 (ru) * | 2003-07-30 | 2008-03-20 | Дзе Проктер Энд Гэмбл Компани | Способ получения натриевой соли 3-пиридил-1-гидроксиэтилиден-1,1-бисфосфиновой кислоты (ризедроната) в кристаллической полупятиводной форме (варианты) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3428524A1 (de) * | 1984-08-02 | 1986-02-13 | Boehringer Mannheim Gmbh, 6800 Mannheim | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| IL77243A (en) * | 1984-12-21 | 1996-11-14 | Procter & Gamble | Pharmaceutical compositions containing geminal diphosphonic acid compounds and certain such novel compounds |
| PH27078A (en) * | 1984-12-21 | 1993-02-01 | Procter & Gamble | Pharmaceutical compositions containing geminal diphosphonates |
| US5641762A (en) * | 1985-05-02 | 1997-06-24 | Research Corporation Technologies, Inc. | Bone targeted inhibitors of carbonic anhydrase |
| DE3540150A1 (de) * | 1985-11-13 | 1987-05-14 | Boehringer Mannheim Gmbh | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| US4902679A (en) * | 1985-12-13 | 1990-02-20 | Norwich Eaton Pharmaceuticals, Inc. | Methods of treating diseases with certain geminal diphosphonates |
| DE3770982D1 (de) * | 1986-04-24 | 1991-08-01 | Fujisawa Pharmaceutical Co | Diphosphonsaeure-verbindungen, verfahren zu deren herstellung und sie enthaltende arzneimittel. |
| DE3626058A1 (de) * | 1986-08-01 | 1988-02-11 | Boehringer Mannheim Gmbh | Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel |
| US5057505A (en) * | 1986-11-21 | 1991-10-15 | Ciba-Geigy Corporation | Substituted aminomethanediphosphonic acids and use in medicaments |
| EP0275821B1 (de) * | 1986-11-21 | 1992-02-26 | Ciba-Geigy Ag | Neue substituierte Alkandiphosphonsäuren |
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| PH9776A (en) * | 1967-12-11 | 1976-03-17 | M Francis | Compositions for inhibiting anomalous deposition and mobilization of calcium phosphate in animal tissue and method of use |
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- 1985-07-26 US US06/759,608 patent/US4687767A/en not_active Expired - Lifetime
- 1985-07-26 AT AT85109432T patent/ATE39489T1/de active
- 1985-07-26 EP EP85109432A patent/EP0170228B1/de not_active Expired
- 1985-07-26 DE DE8585109432T patent/DE3567023D1/de not_active Expired
- 1985-07-30 DK DK345285A patent/DK345285A/da not_active Application Discontinuation
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- 1985-07-30 DD DD85279140A patent/DD236533A5/de not_active IP Right Cessation
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- 1985-07-31 CS CS855580A patent/CS257277B2/cs not_active IP Right Cessation
- 1985-07-31 ZA ZA855760A patent/ZA855760B/xx unknown
- 1985-08-01 HU HU852957A patent/HU196419B/hu not_active IP Right Cessation
- 1985-08-01 FI FI852980A patent/FI78915C/fi not_active IP Right Cessation
- 1985-08-01 SU SU853935742A patent/SU1475487A3/ru active
- 1985-08-01 AU AU45686/85A patent/AU553419B2/en not_active Ceased
- 1985-08-02 JP JP60169944A patent/JPS6143197A/ja active Pending
- 1985-08-02 ES ES545842A patent/ES8606876A1/es not_active Expired
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2124019C1 (ru) * | 1992-05-29 | 1998-12-27 | Дзе Проктер энд Гэмбл Фармасьютикалз, Инк. | Тиозамещенные пиридинилбисфосфоновые кислоты или их фармацевтически приемлемые соли или эфиры, фармацевтическая композиция на их основе и способ лечения |
| RU2154647C2 (ru) * | 1993-08-25 | 2000-08-20 | Мерк Энд Ко., Инк. | ЦИКЛИЧЕСКИЕ ФОСФОРСОДЕРЖАЩИЕ СОЕДИНЕНИЯ И СПОСОБ НЕПРЕРЫВНОГО ПОЛУЧЕНИЯ γ-АМИНО-1-ГИДРОКСИАЛКИЛИДЕН-1,1-БИСФОСФОНОВЫХ КИСЛОТ |
| RU2188011C2 (ru) * | 1995-06-05 | 2002-08-27 | Такеда Кемикал Индастриз, Лтд. | Активирующая остеогенез фармацевтическая композиция |
| RU2236415C2 (ru) * | 2000-02-01 | 2004-09-20 | Дзе Проктер Энд Гэмбл Компани | Способ селективного получения полупентагидрата и моногидрата натриевой соли 3-пиридил -1-гидроксиэтилиден-1,1-бисфосфоновой кислоты и фармацевтическая композиция на их основе |
| RU2319706C2 (ru) * | 2003-07-30 | 2008-03-20 | Дзе Проктер Энд Гэмбл Компани | Способ получения натриевой соли 3-пиридил-1-гидроксиэтилиден-1,1-бисфосфиновой кислоты (ризедроната) в кристаллической полупятиводной форме (варианты) |
Also Published As
| Publication number | Publication date |
|---|---|
| AU4568685A (en) | 1986-02-06 |
| CA1264326A (en) | 1990-01-09 |
| DE3428524A1 (de) | 1986-02-13 |
| DE3567023D1 (en) | 1989-02-02 |
| JPS6143197A (ja) | 1986-03-01 |
| ATE39489T1 (de) | 1989-01-15 |
| ES545842A0 (es) | 1986-05-16 |
| US4687767A (en) | 1987-08-18 |
| DK345285A (da) | 1986-02-03 |
| IL75971A (en) | 1989-05-15 |
| DK345285D0 (da) | 1985-07-30 |
| DD236533A5 (de) | 1986-06-11 |
| IL75971A0 (en) | 1985-12-31 |
| HUT38364A (en) | 1986-05-28 |
| FI852980L (fi) | 1986-02-03 |
| FI78915B (fi) | 1989-06-30 |
| ES8606876A1 (es) | 1986-05-16 |
| FI852980A0 (fi) | 1985-08-01 |
| HU196419B (en) | 1988-11-28 |
| AU553419B2 (en) | 1986-07-17 |
| GR851881B (enExample) | 1985-12-02 |
| CS257277B2 (en) | 1988-04-15 |
| EP0170228B1 (de) | 1988-12-28 |
| FI78915C (fi) | 1989-10-10 |
| EP0170228A1 (de) | 1986-02-05 |
| ZA855760B (en) | 1986-04-30 |
| US4784993A (en) | 1988-11-15 |
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