PH27104A - Process for preparing a naphthalene derivative and a synthetic intermediate thereof - Google Patents

Process for preparing a naphthalene derivative and a synthetic intermediate thereof Download PDF

Info

Publication number
PH27104A
PH27104A PH39989A PH39989A PH27104A PH 27104 A PH27104 A PH 27104A PH 39989 A PH39989 A PH 39989A PH 39989 A PH39989 A PH 39989A PH 27104 A PH27104 A PH 27104A
Authority
PH
Philippines
Prior art keywords
group
ring
formula
compound
salt
Prior art date
Application number
PH39989A
Other languages
English (en)
Inventor
Tameo Iwasaki
Masami Takashi
Hiroshi Ohmizu
Original Assignee
Tanabe Seiyaku Co
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 Tanabe Seiyaku Co filed Critical Tanabe Seiyaku Co
Publication of PH27104A publication Critical patent/PH27104A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/92—Naphthofurans; Hydrogenated naphthofurans
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/70—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with ring systems containing two or more relevant rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04—Ortho-condensed systems
    • 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
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • 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
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Moulding By Coating Moulds (AREA)
  • Water Treatment By Sorption (AREA)
  • Furan Compounds (AREA)
PH39989A 1989-02-03 1990-02-02 Process for preparing a naphthalene derivative and a synthetic intermediate thereof PH27104A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2641689 1989-02-03

Publications (1)

Publication Number Publication Date
PH27104A true PH27104A (en) 1993-03-16

Family

ID=12192938

Family Applications (1)

Application Number Title Priority Date Filing Date
PH39989A PH27104A (en) 1989-02-03 1990-02-02 Process for preparing a naphthalene derivative and a synthetic intermediate thereof

Country Status (14)

Country Link
US (1) US5003087A (fr)
EP (1) EP0380982A3 (fr)
JP (1) JPH02288845A (fr)
CN (1) CN1044649A (fr)
AU (1) AU625546B2 (fr)
BG (1) BG51155A3 (fr)
CA (1) CA2007580A1 (fr)
FI (1) FI900529A7 (fr)
HU (1) HU207279B (fr)
IL (1) IL93070A0 (fr)
NO (1) NO171974C (fr)
PH (1) PH27104A (fr)
PT (1) PT92834A (fr)
ZA (1) ZA9076B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU637500B2 (en) * 1990-06-21 1993-05-27 Zeneca Limited Bicyclic heterocyclic compounds
US5281720A (en) * 1991-02-28 1994-01-25 Merck Frosst Canada, Inc. Pyranylphenyl hydroxyalkylnaphthoic acids as inhibitors of leukotriene biosynthesis
US5227399A (en) * 1991-02-28 1993-07-13 Merck Frosst Canada, Inc. Pyranylphenyl naphthalene lactones as inhibitors of leukotriene biosynthesis
EP0501578A1 (fr) * 1991-02-28 1992-09-02 Merck Frosst Canada Inc. Acides pyranylphényle hydroxyalkylenaphthaléniques et leur utilisation comme inhibiteurs de la biosynthèse de leukotriène
EP0501579A1 (fr) * 1991-02-28 1992-09-02 Merck Frosst Canada Inc. Lactones naphthalèniques comme inhibiteurs de la biosynthèse de leukotriène
US5308852A (en) * 1992-06-29 1994-05-03 Merck Frosst Canada, Inc. Heteroarylnaphthalenes as inhibitors of leukotriene biosynthesis
US5426109A (en) * 1992-08-27 1995-06-20 Merck Frosst Canada, Inc. Phenylnaphthalene hydroxy acids
US5428060A (en) * 1992-08-27 1995-06-27 Merck Frosst Canada, Inc. Heteroarylnaphthalene lactones as inhibitors of leukotriene biosynthesis
US5350744A (en) * 1992-08-27 1994-09-27 Merck Frosst Canada, Inc. Phenylnaphthalene lactones as inhibitors of leukotriene biosynthesis
US5252599A (en) * 1992-08-27 1993-10-12 Merck Frosst Canada, Inc. Heteroarylnaphthalene hydroxy acids as inhibitors of leukotriene biosynthesis
CA2121060C (fr) * 1993-04-16 2004-04-06 Sachio Mori Preparation d'analogues de la lignane
ID18046A (id) * 1996-08-20 1998-02-19 Takeda Chemical Industries Ltd Senyawa siklik campuran, pembuatan dan penngunaannya.
US7754718B2 (en) * 2004-05-05 2010-07-13 Yale University Antiviral helioxanthin analogs
CN106317161B (zh) * 2015-06-29 2020-05-15 深圳翰宇药业股份有限公司 一种氟甲基酮肽系列化合物的制备方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4771072A (en) * 1985-01-10 1988-09-13 Tanabe Seiyaku Co., Ltd. Alkoxynaphthalene derivatives
US4728740A (en) * 1985-04-12 1988-03-01 Bristol-Myers Company Intermediates for the production of epipodophylotoxin and related compounds and processes for the preparation and use thereof
MY105057A (en) * 1989-01-27 1994-07-30 Tanabe Seiyaku Co A process for preparing naphthalene derivatives

Also Published As

Publication number Publication date
IL93070A0 (en) 1990-11-05
HUT53588A (en) 1990-11-28
ZA9076B (en) 1990-10-31
NO171974C (no) 1993-05-26
NO900513D0 (no) 1990-02-02
PT92834A (pt) 1990-08-31
JPH02288845A (ja) 1990-11-28
CA2007580A1 (fr) 1990-08-03
CN1044649A (zh) 1990-08-15
HU900658D0 (en) 1990-04-28
US5003087A (en) 1991-03-26
NO900513L (no) 1990-08-06
FI900529A0 (fi) 1990-02-02
EP0380982A2 (fr) 1990-08-08
EP0380982A3 (fr) 1990-11-28
AU625546B2 (en) 1992-07-16
AU4859090A (en) 1990-08-09
FI900529A7 (fi) 1990-08-04
NO171974B (no) 1993-02-15
HU207279B (en) 1993-03-29
BG51155A3 (bg) 1993-02-15

Similar Documents

Publication Publication Date Title
EP0142146B1 (fr) Analogues oxo du mévinoline utiles comme agents antihypercholestérolémiques
EP0404190B1 (fr) Composés hétérocycliques condensés, leur préparation et leur utilisation
HU219950B (hu) Proteolitikus enzimeket gátló szacharinszármazékok és ezeket tartalmazó gyógyászati készítmények, valamint a szacharinszármazékok előállítása
US5003087A (en) Process for preparing a naphthalene derivative and a synthetic intermediate thereof
HUP0003954A2 (hu) Eljárás és közbenső termékek pirrolo [2,3-d] pirimidin-származékok előállítására
Lam et al. Dihydrocompactin, a new potent inhibitor of 3-hydroxy-3-methylglutaryl coenzyme-A reductase from Penicillium citrinum
KR870006056A (ko) 신규(2-이미다졸린-2-일) 융합 헤테로피리딘 화합물, 그제조방법 및 잡초 억제방법
JPH0832685B2 (ja) ジヒドロピリジン化合物
Houlihan et al. Directed Lithiation of 2-Phenyl-and 2-(o-methylphenyl) imidazoline
JPH0649668B2 (ja) 血中コレステロール低下薬としての３，５−ジヒドロキシ−６，８−ノナジエン酸および誘導体
US5840914A (en) 3-(2-trialkylsilyloxy) ethyl-7-1H-indoles and method for their preparation
EP0905128B1 (fr) Procédés et intermédiaires servant à la préparation d'antifolates
Gais et al. A conceptually new route to optically active carba-prostacyclins: synthesis of exocyclic alkenes via doubly lithiated allyl sulfones
Hatanaka et al. [3+ 2]-Annulation using allylidene (triphenyl) phosphoranes: a one-step synthesis of cyclopentadienes
JP2572774B2 (ja) カルボン酸の合成方法
Chimichi et al. Pyridazine-4, 5-dicarboxylic anhydride: versatile synthon for the preparation of 1, 3, 7, 8-tetra-azaspiro [4.5] decane derivatives with nitrogen 1, 3-binucleophiles
EP0095835A1 (fr) Préparation de 4,7-dialcoxybenzofuranes et des produits intermédiaires utilisés pour cette préparation
US5322941A (en) Process for the preparation of pyrene compounds
RU2123002C1 (ru) Сульфонамидодиоксепаны, способы их получения и фармацевтическая композиция на их основе
US6103914A (en) Method of producing optically active material of tricyclic compound
JPH1072451A (ja) ２−ピリミジンカルボキシレートの製造方法
US4740599A (en) Synthesis of alkylsulfinyl substituted 2-phenylimidazo(4,5-c)pyridines
US4831144A (en) 1H-pyrrolo [3,2-c]pyrrolidines protected in 1-position useful as intermediates
JP3882856B2 (ja) α−フルオロ−β−ケトエステルの製造方法
US5164511A (en) Thioimideazoles useful as intermediates for preparing thiazine