ES2167959T3 - Nafto(2,1-b)piranos fotocromicos fusionados con indeno. - Google Patents

Nafto(2,1-b)piranos fotocromicos fusionados con indeno.

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Publication number
ES2167959T3
ES2167959T3 ES98962926T ES98962926T ES2167959T3 ES 2167959 T3 ES2167959 T3 ES 2167959T3 ES 98962926 T ES98962926 T ES 98962926T ES 98962926 T ES98962926 T ES 98962926T ES 2167959 T3 ES2167959 T3 ES 2167959T3
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ES
Spain
Prior art keywords
alkyl
alkoxy
group
chlorine
mono
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
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ES98962926T
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English (en)
Inventor
Jibing Lin
Gemert Barry Van
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Transitions Optical Inc
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Transitions Optical Inc
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Publication date
Application filed by Transitions Optical Inc filed Critical Transitions Optical Inc
Application granted granted Critical
Publication of ES2167959T3 publication Critical patent/ES2167959T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/20Filters
    • G02B5/22Absorbing filters
    • G02B5/23Photochromic filters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/18Iodine; Compounds thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/02Ethers
    • C07C43/20Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
    • C07C43/23Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/94Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems condensed with rings other than six-membered or with ring systems containing such rings
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31565Next to polyester [polyethylene terephthalate, etc.]
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31598Next to silicon-containing [silicone, cement, etc.] layer
    • Y10T428/31601Quartz or glass
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31721Of polyimide

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Inorganic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Optics & Photonics (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

Un compuesto de naftopirano representado por la siguiente fórmula gráfica: I donde (a) R1 es alcoxi C1-C6; (b) cada R2 es alquilo C1-C3, alcoxi C1-C3, cloro o fluor, y n es el entero 0, 1 ó 2; (c) cada R3 es alquilo C1-C6, cloro o fluor, y m es el entero 0, 1 ó 2; (d) R4 y R5 forman juntos un grupo oxo, o cada uno de R4 y R5 es hidrógeno, hidroxi, alquilo C1-C6, cicloalquilo C3-C7, alilo, fenilo, fenilo monosustituido, bencilo, bencilo monosustituido, o cada uno de R4 y R5 es un grupo -OR6, donde R6 es alquilo C1-C6, fenilalquilo C1-C3, fenilalquilo C1-C3 sustituido con monoalquilo C1-C6, fenilalquilo C1-C3 sustituido con monoalcoxi C1-C6, alcoxi(C1C6)alquilo C2-C4, cicloalquilo C3-C7, cicloalquilo C3-C7 sustituido con monoalquilo C1-C4, cloroalquilo C1-C6, fluoroalquilo C1-C6 o alilo, siendo cada uno de los sustituyentes de dichos grupos fenilo y bencilo alquilo C1-C6 o alcoxiC1-C6; y (e) cada uno de B y B'' se selecciona del grupo formado por: (i) los grupos arilo fenilo y naftilo no sustituidos, mono-, diy trisustituidos; (ii) los grupos hetero aromáticos no sustituidos, monoy disustituidos piridilo, furanilo, benzofuran-2-ilo, benzofuran-3-ilo, tienilo, benzotien-2-ilo, benzotien-3-ilo, estando seleccionados los sustituyentes de dichos grupos arilo y hetero aromático en (e)(i) y (ii) del grupo formado por hidroxi, amino, monoalquil(C1-C6)amino, dialquil(C2-C6)amino, piperidino, morfolino, pirrilo, alquilo C1-C6, cloroalquilo C1-C6,fluoroalquilo C1-C6, alcoxi C1-C6, monoalcoxi(C1-C6)alquilo(C1-C4), acriloxi, metacriloxi, cloro y fluor; (iii) los grupos representados por las siguientes fórmulas gráfics: donde A es carbono u oxígeno y D es oxígeno o nitrógeno sustituido, siempre que cuando D sea nitrógeno sustituido, A es carbono, seleccionándose dichos sustituyentes del nitrógeno del grupo formado por hidrógeno, alquilo C1-C6, y acilo C2-C6; cadaR7 es alquilo C1-C6, alcoxi C1-C6, hidroxi, cloro o úor; cada uno de R8 y R9 es hidrógeno o alquilo C1-C6 y p es el entero 0, 1, ó2; (iv) alquilo C1-C6, cloroalquilo C1-C6, uoroalquilo C1-C6, alcoxi(C1-C6)alquilo C1-C4, cicloalquilo C3-C6, monoalcoxi(C1-C6)cicloalquilo C3-C6, monoalquil(C1-C6)-cicloalquilo C3-C6, clorocicloalquilo C3-C6, y úoro-cicloalquilo C3-C6; y (v) el grupo representado por la siguiente fórmula gráfica: H Q Q í C==C í Q Q Q Z donde Q es hidrógeno o alquilo C1-C4 y Z se selecciona entre los miembros no sustituidos, monoy disustituidos del grupo formado por naftilo, fenilo, furanilo, y tienilo, siendo cada uno de los sustituyentes de dichos grupos alquilo C1-C4, alcoxi C1-C4, fl uor, o cloro; o (vi) B y B'' tomados juntos forman uoren-9-ilideno, uoren-9-ilideno mono-, o disustituido o un miembro seleccionado del grupo formado por los anillos hidrocarbonados espiromonocíclicos C3-C12 saturados; los anillos hidrocarbonados espirobicíclicos C7-C12 saturados; y los anillos hidrocarbonados espirotricíclicos C7-C12 saturados, seleccionándose cada uno de los sustituyentes de dicho uoren-9-ilideno del grupoformado por alquilo C1-C4, alcoxiC1-C4, fluor y cloro.
ES98962926T 1997-12-15 1998-12-07 Nafto(2,1-b)piranos fotocromicos fusionados con indeno. Expired - Lifetime ES2167959T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/990,890 US5869658A (en) 1997-12-15 1997-12-15 Photochromic indeno-fused naptho 2,1-b!pyrans

Publications (1)

Publication Number Publication Date
ES2167959T3 true ES2167959T3 (es) 2002-05-16

Family

ID=25536622

Family Applications (1)

Application Number Title Priority Date Filing Date
ES98962926T Expired - Lifetime ES2167959T3 (es) 1997-12-15 1998-12-07 Nafto(2,1-b)piranos fotocromicos fusionados con indeno.

Country Status (6)

Country Link
US (1) US5869658A (es)
EP (1) EP1042312B1 (es)
AU (1) AU730610B2 (es)
DE (1) DE69802439T2 (es)
ES (1) ES2167959T3 (es)
WO (1) WO1999031083A1 (es)

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FR2794749A1 (fr) 1999-06-10 2000-12-15 Corning Sa Benzopyranes anneles en c7-c8 avec un heterocycle aromatique et les compositions et matrices (co) polymeres les renfermant
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Also Published As

Publication number Publication date
DE69802439D1 (de) 2001-12-13
EP1042312B1 (en) 2001-11-07
AU730610B2 (en) 2001-03-08
EP1042312A1 (en) 2000-10-11
AU1806099A (en) 1999-07-05
WO1999031083A1 (en) 1999-06-24
DE69802439T2 (de) 2002-07-18
US5869658A (en) 1999-02-09

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