FI854797A - Menetelmä terapeuttisesti käyttökelpoisten oksetanonien valmistamiseksi - Google Patents

Menetelmä terapeuttisesti käyttökelpoisten oksetanonien valmistamiseksi Download PDF

Info

Publication number
FI854797A
FI854797A FI854797A FI854797A FI854797A FI 854797 A FI854797 A FI 854797A FI 854797 A FI854797 A FI 854797A FI 854797 A FI854797 A FI 854797A FI 854797 A FI854797 A FI 854797A
Authority
FI
Finland
Prior art keywords
alkyl
opt
ring
oxetanones
substd
Prior art date
Application number
FI854797A
Other languages
English (en)
Swedish (sv)
Other versions
FI91403B (fi
FI854797A0 (fi
FI91403C (fi
Inventor
Pierre Barbier
Fernand Schneider
Ulrich Widmer
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of FI854797A0 publication Critical patent/FI854797A0/fi
Publication of FI854797A publication Critical patent/FI854797A/fi
Publication of FI91403B publication Critical patent/FI91403B/fi
Application granted granted Critical
Publication of FI91403C publication Critical patent/FI91403C/fi

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D305/00Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
    • C07D305/02Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D305/10Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having one or more double bonds between ring members or between ring members and non-ring members
    • C07D305/12Beta-lactones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/10Oxygen atoms
    • C07D309/12Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/16Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D309/28Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D309/30Oxygen atoms, e.g. delta-lactones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804Compounds having Si-O-C linkages
FI854797A 1984-12-21 1985-12-04 Menetelmä terapeuttisesti käyttökelpoisten oksetanonien valmistamiseksi FI91403C (fi)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
CH610284 1984-12-21
CH610284 1984-12-21
CH393485 1985-09-12
CH393485 1985-09-12

Publications (4)

Publication Number Publication Date
FI854797A0 FI854797A0 (fi) 1985-12-04
FI854797A true FI854797A (fi) 1986-06-22
FI91403B FI91403B (fi) 1994-03-15
FI91403C FI91403C (fi) 1994-06-27

Family

ID=25694219

Family Applications (1)

Application Number Title Priority Date Filing Date
FI854797A FI91403C (fi) 1984-12-21 1985-12-04 Menetelmä terapeuttisesti käyttökelpoisten oksetanonien valmistamiseksi

Country Status (20)

Country Link
US (2) US4931463A (fi)
EP (1) EP0185359B1 (fi)
CN (1) CN1012643B (fi)
AT (1) ATE70061T1 (fi)
AU (1) AU583569B2 (fi)
CA (1) CA1270837A (fi)
CS (1) CS262425B2 (fi)
DE (1) DE3584829D1 (fi)
DK (1) DK166724B1 (fi)
DO (1) DOP1985004386A (fi)
FI (1) FI91403C (fi)
HU (1) HU200172B (fi)
IE (1) IE58926B1 (fi)
IL (1) IL77338A (fi)
MC (1) MC1728A1 (fi)
NO (1) NO171160C (fi)
NZ (1) NZ214565A (fi)
PH (1) PH26291A (fi)
PT (1) PT81748B (fi)
ZW (1) ZW20385A1 (fi)

Families Citing this family (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1328881C (en) * 1984-12-21 1994-04-26 Pierre Barbier Process for the manufacture of oxetanones
US5246960A (en) * 1984-12-21 1993-09-21 Hoffmann-La Roche Inc. Oxetanones
US4895973A (en) * 1986-08-14 1990-01-23 G. D. Searle & Company Substituted glutaric acid lactones in the treatment of hyperlipidemia
US4816477A (en) * 1987-05-26 1989-03-28 Merck & Co., Inc. Antihypercholesterolemic β-lactones
US4806564A (en) * 1987-05-26 1989-02-21 Merck & Co., Inc. Antihypercholesterolemic beta-lactones
CA2035972C (en) * 1990-02-23 2006-07-11 Martin Karpf Process for the preparation of oxetanones
US5260310A (en) * 1990-02-26 1993-11-09 Hoffmann-La Roche Inc. Oxetanone compounds and pharmaceutical compositions containing them
CA2098167C (en) * 1992-06-24 2006-12-19 Dorothea Isler Foodstuffs and feedstuffs containing a lipase inhibitor
PT1017408E (pt) * 1997-02-05 2005-07-29 Hoffmann La Roche Utilizacao de tetra-hidrolipstatina no tratamento de diabetes de tipo ii
CN100378118C (zh) 1997-04-15 2008-04-02 Csir公司 具有食欲抑制剂活性的药物组合物
GB2355657B (en) * 1999-10-27 2004-07-28 Phytopharm Plc Inhibitors Of Gastric Acid Secretion
CN1342169A (zh) * 1999-10-29 2002-03-27 约翰·贾森·金特里·穆林斯 氧杂环丁烷酮衍生物
EP1132389A1 (en) 2000-03-06 2001-09-12 Vernalis Research Limited New aza-indolyl derivatives for the treatment of obesity
GB2363985B (en) * 2000-06-30 2004-09-29 Phytopharm Plc Extracts,compounds & pharmaceutical compositions having anti-diabetic activity and their use
CA2416900C (en) * 2000-07-28 2007-07-03 F. Hoffmann-La Roche Ag The use of a combination of a lipase inhibitor and a pharmaceutically acceptable bile acid sequestrant for the prevention and treatment of diseases associated with high plasma cholesterol levels
ES2304132T3 (es) 2000-08-09 2008-09-16 F. Hoffmann-La Roche Ag Inhibidores de lipasa para el tratamiento de la dispepsia.
US6900226B2 (en) 2000-09-06 2005-05-31 Hoffman-La Roche Inc. Neuropeptide Y antagonists
US6392061B1 (en) * 2000-10-16 2002-05-21 Zpro Chemical, Inc. Process for making (2S, 3S, 5S) oxetanone derivatives
CN100334076C (zh) 2000-10-16 2007-08-29 霍夫曼-拉罗奇有限公司 二氢吲哚衍生物及其作为5-ht2受体配体的用途
GB0030710D0 (en) 2000-12-15 2001-01-31 Hoffmann La Roche Piperazine derivatives
CA2432085C (en) 2000-12-27 2009-02-24 F. Hoffmann-La Roche Ag Indole derivatives and their use as 5-ht2b and 5-ht2c receptor ligands
GB0106177D0 (en) 2001-03-13 2001-05-02 Hoffmann La Roche Piperazine derivatives
ES2300478T3 (es) 2001-05-21 2008-06-16 F. Hoffmann-La Roche Ag Derivados de quinolina como ligandos para el receptor de neuropeptido y.
US20030027786A1 (en) 2001-06-06 2003-02-06 Karsten Maeder Lipase inhibiting composition
US6730319B2 (en) 2001-06-06 2004-05-04 Hoffmann-La Roche Inc. Pharmaceutical compositions having depressed melting points
US6787558B2 (en) 2001-09-28 2004-09-07 Hoffmann-La Roche Inc. Quinoline derivatives
GB0202015D0 (en) 2002-01-29 2002-03-13 Hoffmann La Roche Piperazine Derivatives
CA2473181A1 (en) 2002-02-04 2003-08-14 F. Hoffmann-La Roche Ag Quinoline derivatives as npy antagonists
ES2292992T3 (es) 2002-02-28 2008-03-16 F. Hoffmann-La Roche Ag Derivados de tiazol como antagonistas del receptor npy.
WO2003088975A1 (en) * 2002-04-17 2003-10-30 The Burnham Institute Inhibition of fatty acid synthase by beta-lactones and other compounds for inhibition of cellular proliferation
US7728153B2 (en) 2002-04-17 2010-06-01 The Burnham Institute For Medical Research Method for the asymmetric synthesis of beta-lactone compounds
MXPA05000131A (es) 2002-07-05 2005-04-11 Hoffmann La Roche Derivados de quinazolina.
EP1539722A1 (en) 2002-08-07 2005-06-15 F. Hoffmann-La Roche Ag Thiazole derivatives
EP1539746B1 (en) 2002-09-12 2006-11-15 F. Hoffmann-La Roche Ag N-substituted-1h-indol-5-propionic acid compounds as ppar agonists useful for the treatment of diabetes
US6727277B1 (en) 2002-11-12 2004-04-27 Kansas State University Research Foundation Compounds affecting cholesterol absorption
MXPA05005445A (es) 2002-11-25 2005-08-26 Hoffmann La Roche Derivados de indolilo.
GB0314967D0 (en) 2003-06-26 2003-07-30 Hoffmann La Roche Piperazine derivatives
EP1651627A2 (en) * 2003-07-15 2006-05-03 Ranbaxy Laboratories Limited Process for preparation of oxetan-2-ones
CA2533463A1 (en) 2003-08-12 2005-02-17 F. Hoffmann-La Roche Ag 2-amino-5-benzoylthiazole npy antagonists
KR20060037436A (ko) 2003-08-12 2006-05-03 에프. 호프만-라 로슈 아게 Npy 길항물질로서 싸이아졸 유도체
US7074822B2 (en) * 2004-02-23 2006-07-11 Solvay Pharmaceuticals Gmbh Alkyl carbamate-substituted β-lactones, process for their preparation, and pharmaceutical compositions containing them
DE102004009076A1 (de) * 2004-02-23 2005-10-27 Solvay Pharmaceuticals Gmbh Alkylcarbamat-substituierte β-Lactone, Verfahren und Zwischenprodukte zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
US7121355B2 (en) * 2004-09-21 2006-10-17 Cnh America Llc Bulldozer autograding system
WO2006035296A1 (en) * 2004-09-27 2006-04-06 Ranbaxy Laboratories Limited Process for the preparation of an orlistat derivative useful as reference standard in the determination of the purity of orlistat and process for the preparation of orlistat
KR100895758B1 (ko) 2005-05-03 2009-04-30 에프. 호프만-라 로슈 아게 5-ht2 리간드로서 테트라사이클릭 아자피라지노인돌린
ATE430744T1 (de) 2005-08-18 2009-05-15 Hoffmann La Roche Thiazolylpiperidin-derivate nützlich als h3 rezeptor modulatoren
US20090171104A1 (en) * 2005-10-05 2009-07-02 Killol Patel Process for the preparation of orlistat
AU2006319235A1 (en) 2005-11-30 2007-06-07 F. Hoffmann-La Roche Ag 5-substituted indole-2-carboxamide derivatives
WO2007062999A2 (en) 2005-11-30 2007-06-07 F. Hoffmann-La Roche Ag 1,5-substituted indol-2-yl amide derivatives
DE602006021626D1 (de) 2005-11-30 2011-06-09 Hoffmann La Roche 1,1-dioxo-thiomorpholinyl-indolyl-methanon-derivate zur verwendung als h3-modulatoren
CN101321761A (zh) 2005-12-09 2008-12-10 霍夫曼-拉罗奇有限公司 用于治疗肥胖病的三环酰胺衍生物
EP1963318B1 (en) 2005-12-15 2009-11-25 F. Hoffmann-la Roche AG Pyrrolo[2,3-c]pyridine derivatives
AU2006326067A1 (en) 2005-12-16 2007-06-21 F. Hoffmann-La Roche Ag Pyrrolo [2 , 3-b] pyridine derivatives as H3 receptor modulators
EP1976840A1 (en) * 2006-01-13 2008-10-08 F.Hoffmann-La Roche Ag Cyclohexyl piperazinyl methanone derivatives and their use as histamine h3 receptor modulators
CN101370779B (zh) * 2006-01-23 2011-07-20 霍夫曼-拉罗奇有限公司 具有h3受体活性的环己基磺酰胺衍生物
US7432255B2 (en) 2006-05-16 2008-10-07 Hoffmann-La Roche Inc. 1H-indol-5-yl-piperazin-1-yl-methanone derivatives
CA2652158A1 (en) * 2006-05-30 2007-12-06 Matthias Heinrich Nettekoven Piperidinyl pyrimidine derivatives
US7514433B2 (en) 2006-08-03 2009-04-07 Hoffmann-La Roche Inc. 1H-indole-6-yl-piperazin-1-yl-methanone derivatives
US20080146559A1 (en) 2006-12-08 2008-06-19 Li Chen 4,5,6,7-Tetrahydro-Thieno [2,3-C] Pyridine Derivatives
SG182171A1 (en) * 2007-06-06 2012-07-30 Ranbaxy Lab Ltd Process for the preparation of orlistat
EP2183237A1 (en) 2007-07-25 2010-05-12 F. Hoffmann-Roche AG Benzofuran- and benzo[b]thiophene-2-carboxylic acid amide derivatives and use thereof as histamine 3 receptor modulators
EP2212305A4 (en) * 2007-10-31 2011-10-26 Burnham Inst Medical Research BETA-LACTONE COMPOUNDS
WO2010112569A1 (en) 2009-03-31 2010-10-07 Robert Zimmermann Modulation of adipose triglyceride lipase for prevention and treatment of cachexia, loss of weight and muscle atrophy and methods of screening therefor
WO2010115825A2 (en) 2009-03-31 2010-10-14 Robert Zimmermann Modulation of adipose triglyceride lipase for prevention and treatment of cachexia, loss of weight and muscle atrophy and methods of screening therefor
CA2798330A1 (en) 2010-05-05 2011-11-10 Infinity Pharmaceuticals, Inc. Tetrazolones as inhibitors of fatty acid synthase
US8450350B2 (en) 2010-05-05 2013-05-28 Infinity Pharmaceuticals, Inc. Triazoles as inhibitors of fatty acid synthase
EP4218753A3 (en) 2017-07-12 2023-10-11 Mayo Foundation for Medical Education and Research Compounds for the reducing lipotoxic damage
CN112079821A (zh) * 2020-09-14 2020-12-15 中山万汉制药有限公司 奥利司他与苯氨基嘧啶类化合物形成的缀合物及其制备方法与用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2478388A (en) * 1945-09-28 1949-08-09 Eastman Kodak Co beta-lactones from unsaturated aldehydes and unsaturated ketones
JPS608117B2 (ja) * 1977-02-08 1985-02-28 財団法人微生物化学研究会 新生理活性物質エステラスチンおよびその製造法
GB2023604B (en) * 1978-05-25 1982-07-28 Microbial Chem Res Found Physiologically active derivatives of esterastin and production thereof
JPS5587720A (en) * 1978-12-27 1980-07-02 Meiji Seika Kaisha Ltd Anti-inflammatory agent
JPS56128774A (en) * 1980-03-14 1981-10-08 Microbial Chem Res Found New physiologically active substance ebelactone and its preparation
CA1247547A (en) * 1983-06-22 1988-12-28 Paul Hadvary Leucine derivatives

Also Published As

Publication number Publication date
US4931463A (en) 1990-06-05
CS262425B2 (en) 1989-03-14
EP0185359A3 (en) 1987-08-26
CN1012643B (zh) 1991-05-22
EP0185359A2 (de) 1986-06-25
IL77338A (en) 1991-04-15
NZ214565A (en) 1989-06-28
US5175186A (en) 1992-12-29
PT81748B (pt) 1988-07-29
PH26291A (en) 1992-04-10
DK600385D0 (da) 1985-12-20
PT81748A (en) 1986-01-02
AU583569B2 (en) 1989-05-04
DK166724B1 (da) 1993-07-05
HUT39440A (en) 1986-09-29
DE3584829D1 (de) 1992-01-16
EP0185359B1 (de) 1991-12-04
NO171160B (no) 1992-10-26
CA1270837A (en) 1990-06-26
DOP1985004386A (es) 1991-04-20
IE853277L (en) 1986-06-21
AU5125985A (en) 1986-06-26
MC1728A1 (fr) 1986-12-15
FI91403B (fi) 1994-03-15
NO855213L (no) 1986-06-23
DK600385A (da) 1986-06-22
FI854797A0 (fi) 1985-12-04
ZW20385A1 (en) 1986-03-05
FI91403C (fi) 1994-06-27
NO171160C (no) 1993-02-03
HU200172B (en) 1990-04-28
ATE70061T1 (de) 1991-12-15
IE58926B1 (en) 1993-12-01
CN85108888A (zh) 1986-07-09

Similar Documents

Publication Publication Date Title
FI854797A (fi) Menetelmä terapeuttisesti käyttökelpoisten oksetanonien valmistamiseksi
DE3575130D1 (de) Antiinflammatorische 1,n-diarylpyrazol-3-amine, deren zusammensetzungen und verfahren zu deren herstellung.
DE19575040I2 (de) 2-Beta-morpholino androstanderivate und Verfahren zu ihrer Herstellung
GR850309B (fi)
ES9100003A1 (es) Un procedimiento para la preparacion de oxetanonas.
ATE66604T1 (de) Penem- oder carbapenemantibiotikum enthaltende zusammensetzung.
DE3669413D1 (de) Doppelsperrverbindung zur befestigung des kopfstueckes mit den fuehrungsrohren eines kernbrennstabbuendels.
ATE114973T1 (de) Hepatocyt-stimulierender faktor.
ATE84717T1 (de) Verwendung von 6-methylen-6-desoxy-nus850906
ES454888A1 (es) Un procedimiento para la preparacion de nuevos cromados.
DK0533209T3 (da) Farmaceutisk præparat indeholdende protein C som beta-sympatomimetikum.
FR2263750A1 (en) N-phenyl-N-(2-aryl-6-methyl-pyrimidin-4-yl)amino acid derivs. - useful e.g. as analeptics, hypotensives, analgesics, etc.
ES8604879A1 (es) Un procedimiento para la preparacion de nuevos derivados de tiocetena
ES8705862A1 (es) Un procedimiento para la preparacion de nuevos derivados de tiocetena
NL7803421A (en) Omega-cycloalkyl prostaglandin derivs. - useful as selective and long lasting vasodepressors, smooth muscle stimulants, CNS active agents, hypotensives, bronchodilators, etc.
IT1130554B (it) Mercapto acil-derivati della prolina e dell'acido pipecolico cheto-sostituti
CS262989A2 (en) Method of new substituted 2,4-diamino-5-cyanopyrimidines production
TH3698EX (th) สารผสมล้างปาก
ES8800141A1 (es) Un procedimiento para preparar un derivado de semicarbazida
NL7812533A (en) (N)-3-Mercapto-2-methyl-propionyl thiazolidinyl-4-carboxylic acids - useful as carboxy-peptidase inhibitors used to treat hypertension

Legal Events

Date Code Title Description
BB Publication of examined application
FG Patent granted

Owner name: F. HOFFMANN-LA ROCHE AG

MA Patent expired