FI107608B - Menetelmä antifungaalisen yhdisteen valmistamiseksi sekä menetelmässä käytettävät välituotteet - Google Patents
Menetelmä antifungaalisen yhdisteen valmistamiseksi sekä menetelmässä käytettävät välituotteet Download PDFInfo
- Publication number
- FI107608B FI107608B FI910508A FI910508A FI107608B FI 107608 B FI107608 B FI 107608B FI 910508 A FI910508 A FI 910508A FI 910508 A FI910508 A FI 910508A FI 107608 B FI107608 B FI 107608B
- Authority
- FI
- Finland
- Prior art keywords
- compound
- formula
- process according
- reduction
- triazol
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/30—Halogen atoms or nitro radicals
-
- 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
- A61P31/04—Antibacterial agents
-
- 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
- A61P31/10—Antimycotics
-
- 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
- C07D213/61—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FI971238A FI971238A (fi) | 1990-02-02 | 1997-03-25 | Triatsolisienitautilääkkeet |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB909002375A GB9002375D0 (en) | 1990-02-02 | 1990-02-02 | Triazole antifungal agents |
GB9002375 | 1990-02-02 |
Publications (3)
Publication Number | Publication Date |
---|---|
FI910508A0 FI910508A0 (fi) | 1991-02-01 |
FI910508A FI910508A (fi) | 1991-08-03 |
FI107608B true FI107608B (fi) | 2001-09-14 |
Family
ID=10670334
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI910508A FI107608B (fi) | 1990-02-02 | 1991-02-01 | Menetelmä antifungaalisen yhdisteen valmistamiseksi sekä menetelmässä käytettävät välituotteet |
FI971238A FI971238A (fi) | 1990-02-02 | 1997-03-25 | Triatsolisienitautilääkkeet |
FI20000084A FI20000084A (fi) | 1990-02-02 | 2000-01-17 | Menetelmä sieniä tuhoavan farmaseuttisen koostumuksen valmistamiseksi |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI971238A FI971238A (fi) | 1990-02-02 | 1997-03-25 | Triatsolisienitautilääkkeet |
FI20000084A FI20000084A (fi) | 1990-02-02 | 2000-01-17 | Menetelmä sieniä tuhoavan farmaseuttisen koostumuksen valmistamiseksi |
Country Status (42)
Country | Link |
---|---|
US (2) | US5567817A (lv) |
EP (1) | EP0440372B1 (lv) |
JP (2) | JP2625584B2 (lv) |
KR (1) | KR930011039B1 (lv) |
CN (2) | CN1026788C (lv) |
AP (2) | AP9000237A0 (lv) |
AT (1) | ATE90090T1 (lv) |
AU (1) | AU625188B2 (lv) |
BA (1) | BA97298A (lv) |
BG (1) | BG60032B2 (lv) |
BR (1) | BR9100435A (lv) |
CA (2) | CA2285891C (lv) |
CZ (1) | CZ279339B6 (lv) |
DE (2) | DE10299035I2 (lv) |
DK (1) | DK0440372T3 (lv) |
EG (1) | EG19750A (lv) |
ES (1) | ES2055523T4 (lv) |
FI (3) | FI107608B (lv) |
GB (1) | GB9002375D0 (lv) |
HK (1) | HK219396A (lv) |
HU (2) | HU205351B (lv) |
IE (1) | IE64774B1 (lv) |
IL (2) | IL97045A (lv) |
IN (1) | IN176148B (lv) |
IS (1) | IS1629B (lv) |
LU (1) | LU90960I2 (lv) |
LV (1) | LV10615B (lv) |
MA (1) | MA22054A1 (lv) |
MX (1) | MX24363A (lv) |
MY (1) | MY105494A (lv) |
NL (1) | NL300100I2 (lv) |
NO (2) | NO176796C (lv) |
NZ (1) | NZ247205A (lv) |
OA (1) | OA09480A (lv) |
PE (1) | PE31691A1 (lv) |
PL (3) | PL169307B1 (lv) |
PT (1) | PT96617B (lv) |
RO (1) | RO109648B1 (lv) |
RU (2) | RU2114838C1 (lv) |
SK (1) | SK278215B6 (lv) |
YU (1) | YU48105B (lv) |
ZA (1) | ZA91761B (lv) |
Families Citing this family (66)
Publication number | Priority date | Publication date | Assignee | Title |
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GB9002375D0 (en) * | 1990-02-02 | 1990-04-04 | Pfizer Ltd | Triazole antifungal agents |
GB9121456D0 (en) * | 1991-10-10 | 1991-11-27 | Pfizer Ltd | Triazole antifungal agents |
GB2281297A (en) * | 1993-08-27 | 1995-03-01 | Merck & Co Inc | Quinazoline compounds |
NZ270418A (en) * | 1994-02-07 | 1997-09-22 | Eisai Co Ltd | Polycyclic triazole & imidazole derivatives, antifungal compositions |
DE19500379A1 (de) * | 1995-01-09 | 1996-07-11 | Basf Ag | Fluorierte Pyrimidine als Herbizide |
GB9516121D0 (en) * | 1995-08-05 | 1995-10-04 | Pfizer Ltd | Organometallic addition to ketones |
GB9602080D0 (en) * | 1996-02-02 | 1996-04-03 | Pfizer Ltd | Pharmaceutical compounds |
GB9605705D0 (en) * | 1996-03-19 | 1996-05-22 | Pfizer Ltd | Therapeutic agents |
US7193083B2 (en) * | 1996-07-26 | 2007-03-20 | Pfizer, Inc. | Preparation of triazoles by organometallic addition to ketones and intermediates therefor |
GB9713149D0 (en) * | 1997-06-21 | 1997-08-27 | Pfizer Ltd | Pharmaceutical formulations |
CN1081189C (zh) * | 1998-07-17 | 2002-03-20 | 国家医药管理局四川抗菌素工业研究所 | 唑醇类新衍生物及其制备方法和医药用途 |
GB9818258D0 (en) * | 1998-08-21 | 1998-10-14 | Pfizer Ltd | Antifungal compositions |
JP2003501488A (ja) * | 1999-06-11 | 2003-01-14 | ネオルックス コーポレイション | 骨髄抑制のための高投与量放射性核種錯体 |
US7094885B2 (en) * | 1999-07-11 | 2006-08-22 | Neorx Corporation | Skeletal-targeted radiation to treat bone-associated pathologies |
US6391903B1 (en) * | 1999-09-09 | 2002-05-21 | Sankyo Company, Limited | Triazole derivatives having antifungal activity |
US6319933B1 (en) | 2000-04-17 | 2001-11-20 | Basilea Pharmaceutica Ag | Azole derivatives |
WO2003079972A2 (en) | 2002-02-22 | 2003-10-02 | New River Parmaceuticals Inc. | Active agent delivery systems and methods for protecting and administering active agents |
AU2002249935A1 (en) * | 2001-01-08 | 2002-08-19 | Neorx Corporation | Radioactively labelled conjugates of phosphonates |
HUP0303249A3 (en) | 2001-02-22 | 2007-03-28 | Sankyo Co | Water-soluble triazole fungicide compounds and pharmaceutical compositions containing them |
US7045116B2 (en) | 2001-12-13 | 2006-05-16 | Dow Global Technologies Inc. | Treatment of osteomyelitis with radiopharmaceuticals |
CN100579977C (zh) * | 2002-10-08 | 2010-01-13 | 许永翔 | 制备三唑类抗真菌药物的方法 |
US20040098839A1 (en) * | 2002-11-27 | 2004-05-27 | Pfizer Inc. | Crystallization method and apparatus using an impinging plate assembly |
US20080194820A1 (en) * | 2004-12-14 | 2008-08-14 | Venkataraman Sundaram | Process For Preparing Voriconazole |
KR101048535B1 (ko) | 2005-03-30 | 2011-07-11 | 주식회사 대웅제약 | 항진균성 트리아졸 유도체 |
WO2007132354A2 (en) * | 2006-02-01 | 2007-11-22 | Medichem, S.A. | Process for preparing voriconazole, new polymorphic form of intermediate thereof, and uses thereof |
AR061889A1 (es) * | 2006-07-13 | 2008-10-01 | Medichem Sa | Proceso mejorado para la preparacion de voriconazol |
CN1919846B (zh) * | 2006-09-14 | 2013-01-02 | 大道隆达(北京)医药科技发展有限公司 | 伏立康唑及其药用盐、中间体的一种新定向合成制备方法 |
CA2669887A1 (en) * | 2006-11-21 | 2008-05-29 | Viamet Pharmaceuticals, Inc. | Metallo-oxidoreductase inhibitors using metal binding moieties in combination with targeting moieties |
KR100889937B1 (ko) | 2007-08-06 | 2009-03-20 | 한미약품 주식회사 | 보리코나졸의 제조방법 |
GB2452049A (en) * | 2007-08-21 | 2009-02-25 | Alpharma Aps | Process for the preparation of voriconazole |
CN101575330B (zh) * | 2008-05-05 | 2012-10-31 | 丽珠医药集团股份有限公司 | 伏立康唑广谱抗真菌药物化合物、其组合物及用途 |
US20110224232A1 (en) * | 2008-05-06 | 2011-09-15 | Board Of Regents, The University Of Texas System | Treatment of Pulmonary Fungal Infection With Voriconazole via Inhalation |
JP2009286756A (ja) | 2008-05-30 | 2009-12-10 | Fujifilm Finechemicals Co Ltd | トリアゾール誘導体またはその塩 |
MX2010013363A (es) * | 2008-06-06 | 2011-03-03 | Glenmark Pharmaceuticals Ltd | Formulacion topica estable contiene voriconazol. |
US20110312977A1 (en) * | 2009-02-17 | 2011-12-22 | Glenmark Generics Limited | Process for the preparation of voriconazole |
KR101109215B1 (ko) | 2009-06-17 | 2012-01-30 | 보령제약 주식회사 | 보리코나졸의 신규 중간체 및 이를 이용한 보리코나졸의 제조방법 |
WO2011020605A1 (en) | 2009-08-19 | 2011-02-24 | Ratiopharm Gmbh | Process for the production of coevaporates and complexes comprising voriconazole and cyclodextrin |
SG10201405886WA (en) | 2009-10-01 | 2014-11-27 | Adare Pharmaceuticals Inc | Orally administered corticosteroid compositions |
WO2011064558A2 (en) | 2009-11-30 | 2011-06-03 | Cipla Limited | Pharmaceutical composition |
JP2013516394A (ja) | 2009-12-30 | 2013-05-13 | メディケム ソシエダ アノニマ | 医薬用途用の1−(1h−1,2,4−トリアゾール−1−イル)ブタン−2−オール誘導体、および前記1−(1h−1,2,4−トリアゾール−1−イル)ブタン−2−オール誘導体を調製するための、実質的に不定の結晶形状を有する1−(1h−1,2,4−トリアゾール−1−イル)ブタン−2−オール誘導体の使用 |
KR100971371B1 (ko) * | 2010-02-04 | 2010-07-20 | 동국제약 주식회사 | 신규한 중간체를 이용한 보리코나졸의 제조방법 |
WO2011110198A1 (en) | 2010-03-10 | 2011-09-15 | Synthron B.V. | A process for making voriconazole |
EP2409699B1 (en) * | 2010-07-23 | 2014-04-30 | Combino Pharm, S.L. | Stable compositions of voriconazole |
CN101914091B (zh) * | 2010-07-25 | 2015-05-27 | 浙江华海药业股份有限公司 | 一种制备伏立康唑中间体的方法 |
PL2678333T3 (pl) | 2011-02-21 | 2015-08-31 | Ranbaxy Laboratories Ltd | Ulepszony sposób otrzymywania worykonazolu i jego produktów pośrednich |
PL2720723T3 (pl) | 2011-06-15 | 2018-10-31 | Synthon Bv | Stabilizowana kompozycja worykonazolu |
EP2561863A1 (en) | 2011-08-22 | 2013-02-27 | Farmaprojects, S.A.U. | Pharmaceutical compositions comprising voriconazole |
US20150133472A1 (en) | 2012-05-11 | 2015-05-14 | Cipla Limited | Pharmaceutical composition |
PT2906555T (pt) | 2012-10-15 | 2017-02-15 | Pfizer Ireland Pharmaceuticals | Processo para a preparação de voriconazol e análogos do mesmo |
JP6404235B2 (ja) * | 2013-02-04 | 2018-10-10 | シンジェンタ パーティシペーションズ アーゲー | 新規な殺微生物剤 |
WO2015034678A2 (en) | 2013-09-06 | 2015-03-12 | Aptalis Pharmatech, Inc. | Corticosteroid containing orally disintegrating tablet compositions for eosinophilic esophagitis |
JP6262972B2 (ja) * | 2013-09-17 | 2018-01-17 | 公益財団法人微生物化学研究会 | 化合物、及びその製造方法、並びにボリコナゾールの製造方法 |
EP3277674B1 (en) | 2015-04-02 | 2019-09-11 | Bayer CropScience Aktiengesellschaft | Triazol derivatives as fungicides |
CN104987325B (zh) * | 2015-06-30 | 2017-03-29 | 扬子江药业集团南京海陵药业有限公司 | 一种伏立康唑的制备方法 |
CN106117186B (zh) * | 2016-06-12 | 2018-08-24 | 重庆莱美隆宇药业有限公司 | 一种伏立康唑及其中间体的制备方法 |
CN107556294A (zh) * | 2016-06-30 | 2018-01-09 | 陕西合成药业股份有限公司 | 一种新型抗真菌感染药物及其制备方法和用途 |
TWI777515B (zh) | 2016-08-18 | 2022-09-11 | 美商愛戴爾製藥股份有限公司 | 治療嗜伊紅性食道炎之方法 |
IL287622B (en) * | 2016-11-28 | 2022-07-01 | Cellix Bio Private Ltd | Preparations and methods for treating fungal infections |
US11185548B2 (en) | 2016-12-23 | 2021-11-30 | Helmholtz Zentrum Munchen—Deutsches Forschungszentrum Für Gesundheit Und Umwelt (Gmbh) | Inhibitors of cytochrome P450 family 7 subfamily B member 1 (CYP7B1) for use in treating diseases |
EP3584245A4 (en) * | 2017-02-17 | 2020-08-26 | Wuhan LL Science And Technology Development Co., Ltd. | TRIAZOLE ANTIBACTERIAL DERIVATIVE, ASSOCIATED PHARMACEUTICAL COMPOSITION AND USE |
CN109705102A (zh) | 2019-02-19 | 2019-05-03 | 浙江华海立诚药业有限公司 | 伏立康唑及其中间体的制备方法 |
CN111440152B (zh) * | 2020-05-18 | 2022-09-27 | 浙江诚意药业股份有限公司 | 一种伏立康唑的制备方法 |
CN112079819B (zh) * | 2020-09-24 | 2022-06-17 | 南京易亨制药有限公司 | 一种改进的伏立康唑消旋体制备方法 |
CN114907319B (zh) * | 2021-02-06 | 2024-06-14 | 华创合成制药股份有限公司 | 一种氘代三唑类化合物及其制备方法和用途 |
CN115724829A (zh) * | 2022-12-23 | 2023-03-03 | 天津力生制药股份有限公司 | 一种分离真菌药物中间体杂质的液相色谱制备方法 |
CN118307408A (zh) * | 2024-04-10 | 2024-07-09 | 上海恩氟佳科技有限公司 | 2-氟丙酰乙酸乙酯的制备方法 |
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