CH521935A - Verfahren zur Herstellung von 2-(6'-Methoxy-2'-naphthyl)propanal und Verwendung desselben - Google Patents

Verfahren zur Herstellung von 2-(6'-Methoxy-2'-naphthyl)propanal und Verwendung desselben

Info

Publication number
CH521935A
CH521935A CH1096269A CH1096269A CH521935A CH 521935 A CH521935 A CH 521935A CH 1096269 A CH1096269 A CH 1096269A CH 1096269 A CH1096269 A CH 1096269A CH 521935 A CH521935 A CH 521935A
Authority
CH
Switzerland
Prior art keywords
propanal
naphthyl
methoxy
preparation
same
Prior art date
Application number
CH1096269A
Other languages
English (en)
Inventor
Harold Nelson Peter
Original Assignee
Syntex Corp
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 Syntex Corp filed Critical Syntex Corp
Priority to CH1868271A priority Critical patent/CH545264A/de
Publication of CH521935A publication Critical patent/CH521935A/de

Links

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
    • C07F9/535—Organo-phosphoranes
    • C07F9/5352—Phosphoranes containing the structure P=C-
    • 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
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • 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]
    • 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
    • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
    • C07C45/513—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an etherified hydroxyl group
    • 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
    • C07F9/54—Quaternary phosphonium compounds
    • C07F9/5407—Acyclic saturated phosphonium compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pain & Pain Management (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Rheumatology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
CH1096269A 1968-07-24 1969-07-17 Verfahren zur Herstellung von 2-(6'-Methoxy-2'-naphthyl)propanal und Verwendung desselben CH521935A (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CH1868271A CH545264A (de) 1968-07-24 1969-07-17 Verfahren zur Herstellung der 2-(6'-Methoxy-2'-naphthyl)-propionsäure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US74707168A 1968-07-24 1968-07-24

Publications (1)

Publication Number Publication Date
CH521935A true CH521935A (de) 1972-04-30

Family

ID=25003550

Family Applications (1)

Application Number Title Priority Date Filing Date
CH1096269A CH521935A (de) 1968-07-24 1969-07-17 Verfahren zur Herstellung von 2-(6'-Methoxy-2'-naphthyl)propanal und Verwendung desselben

Country Status (7)

Country Link
US (1) US3562336A (de)
JP (2) JPS5231868B1 (de)
CH (1) CH521935A (de)
ES (1) ES368572A1 (de)
IL (1) IL32225A (de)
NL (1) NL160485C (de)
SE (1) SE382045B (de)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4207241A (en) * 1967-01-13 1980-06-10 Syntex Corporation 2-Naphthyl acetic acid derivatives and compositions and methods thereof
US3681432A (en) * 1969-09-30 1972-08-01 Syntex Corp 2-formyl-(6-methoxy-2-naphthyl) acetic acid
BR6915468D0 (pt) * 1969-10-09 1973-03-13 Syntex Corp Processo para a preparacao de d 2-(6-substituido-2-naftil)-propanal
US4001301A (en) * 1971-11-04 1977-01-04 Syntex Corporation 6-substituted 2-naphthyl acetic acid derivatives
US3969415A (en) * 1971-12-01 1976-07-13 Sandoz, Inc. 1-(2-Naphthyl)-2,3-butadien-1-ols
US3873718A (en) * 1973-03-29 1975-03-25 Syntex Corp Method for delaying the onset of, or postponing, parturition
US3943257A (en) * 1973-08-20 1976-03-09 Sandoz, Inc. 4-Alkyl-4-naphthyl butenes
US3994968A (en) * 1975-01-10 1976-11-30 Syntex Corporation 2-(5'-Halo-6'-methoxynaphth-2'-yl)-acrylic acid
US4912248A (en) * 1987-05-18 1990-03-27 The Procter & Gamble Company Novel anti-inflammatory agents, pharmaceutical compositions and methods for reducing inflammation
US5286902A (en) * 1991-04-15 1994-02-15 Koch Industries, Inc. Process for preparation of 2-(6-methoxy-2-naphthyl)propionic acid and intermediates therefor utilizing 2,6-diisopropylnaphthalene
US6096920A (en) * 1997-01-08 2000-08-01 Albemarle Corporation Preparation of carboxylic compounds and their derivatives
US6080888A (en) * 1997-01-08 2000-06-27 Albemarle Corporation Preparation of olefinic compounds and carboxylic derivatives thereof
US5792886A (en) * 1997-01-08 1998-08-11 Albemarle Corporation Production of racemic 2-(6-methoxy-2-naphthyl) propionic acid of precursors thereof
US5874614A (en) * 1997-12-11 1999-02-23 Albemarle Corporation Sodium (S)-2-(6-methoxy-2-naphthyl)propionate monohydrate
US5859292A (en) * 1997-12-11 1999-01-12 Albemarle Corporation Preparation of high purity sodium (S)-2(6-methoxy-2-naphthyl)propionate
CN1675154A (zh) * 2002-06-07 2005-09-28 科蒂科股份有限公司 抑制巨噬细胞移动抑制因子(mif)的细胞因子或生物活性的萘衍生物

Also Published As

Publication number Publication date
NL160485C (nl) 1979-11-15
JPS5241258B1 (de) 1977-10-17
JPS5231868B1 (de) 1977-08-17
SE382045B (sv) 1976-01-12
NL6911089A (de) 1970-01-27
IL32225A0 (en) 1969-07-30
ES368572A1 (es) 1971-05-01
IL32225A (en) 1973-08-29
NL160485B (nl) 1979-06-15
US3562336A (en) 1971-02-09

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Legal Events

Date Code Title Description
PUE Assignment

Owner name: SYNTEX PHARMACEUTICALS INTERNATIONAL LIMITED

PL Patent ceased