ES2179480T3 - 3h-nafto(2,1-b)piranos hipercromicos de coloracion roja. - Google Patents

3h-nafto(2,1-b)piranos hipercromicos de coloracion roja.

Info

Publication number
ES2179480T3
ES2179480T3 ES98914972T ES98914972T ES2179480T3 ES 2179480 T3 ES2179480 T3 ES 2179480T3 ES 98914972 T ES98914972 T ES 98914972T ES 98914972 T ES98914972 T ES 98914972T ES 2179480 T3 ES2179480 T3 ES 2179480T3
Authority
ES
Spain
Prior art keywords
sup
alkyl
hyperchromical
nafto
pyranes
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
Application number
ES98914972T
Other languages
English (en)
Inventor
David A Clarke
Bernard Mark Heron
Christopher David Gabbutt
John David Hepworth
Steven Michael Partington
Stephen Nigel Corns
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
James Robinson Speciality Ingredients Ltd
Original Assignee
James Robinson Ltd
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 James Robinson Ltd filed Critical James Robinson Ltd
Application granted granted Critical
Publication of ES2179480T3 publication Critical patent/ES2179480T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C07D405/10—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 aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic 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
    • C07D311/78—Ring systems having three or more relevant rings
    • C07D311/92—Naphthopyrans; Hydrogenated naphthopyrans

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

La invención se refiere a compuestos colorantes rojos hipercrómicos de fórmula general (I), en la que R{sup,1} es H, NR{sup,2}R{sup,3}, OR{sup,4}, SR{sup,4} o R{sup,7} en la que R{sup,2} y R{sup,3} son grupos alquílicos o carbocíclicos o junto con el nitrógeno al que están enlazados forman un anillo heterocíclico; R{sup,4} es igual a R{sup,1} o es alquilo, perhaloalilo, arilo o heteroarilo; R{sup,7} es alquilo, haloalquilo, alquiltio, arilo, ariltio, heteroarilo, halógeno, nitrilo, carboxilato, éster, nitro o un anillo carbocíclico o heterocíclico fusionado a las caras f, g,h, i, j o k; y R{sup,5} es una grupo aminoarilo cíclico, un grupo indolinoarilo, un heterociclo tricíclico con nitrógeno o un grupo aminoarilo cíclico insaturado.
ES98914972T 1997-04-04 1998-04-03 3h-nafto(2,1-b)piranos hipercromicos de coloracion roja. Expired - Lifetime ES2179480T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9706939.7A GB9706939D0 (en) 1997-04-04 1997-04-04 Red colouring hyperchromic 3H-naptho[2,1-6]pyrans

Publications (1)

Publication Number Publication Date
ES2179480T3 true ES2179480T3 (es) 2003-01-16

Family

ID=10810343

Family Applications (1)

Application Number Title Priority Date Filing Date
ES98914972T Expired - Lifetime ES2179480T3 (es) 1997-04-04 1998-04-03 3h-nafto(2,1-b)piranos hipercromicos de coloracion roja.

Country Status (8)

Country Link
US (1) US6294112B1 (es)
EP (1) EP0973761B1 (es)
JP (1) JP4324661B2 (es)
DE (1) DE69806367T2 (es)
DK (1) DK0973761T3 (es)
ES (1) ES2179480T3 (es)
GB (2) GB9706939D0 (es)
WO (1) WO1998045281A1 (es)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9726361D0 (en) * 1997-12-12 1998-02-11 James Robinson Ltd Photochromic dyes
DE19913687A1 (de) * 1998-03-25 1999-12-02 Rodenstock Optik G Photochrome Diaryl-Naphthopyrane mit zumindest einem aminosubstituierten Arylrest
US6478988B1 (en) 1998-12-31 2002-11-12 Bmc Vision-Ease Lens, Inc. Photochromic substituted naphthopyran compounds
US6719926B2 (en) * 1999-06-03 2004-04-13 Tokuyama Corporation Chromene compound
EP1122251B1 (en) * 1999-06-03 2005-07-20 Tokuyama Corporation Chromene compounds
US6312811B1 (en) * 1999-07-08 2001-11-06 Essilor International Compagnie Generale D'optique Photochromic naphtho [2,1-b]pyran compounds containing bithienyl or terthienyl substituents, process for their manufacture, and photochromic materials and articles obtained
GB9918951D0 (en) * 1999-08-11 1999-10-13 James Robinson Ltd Rapid fading photo-responsive materials
US6340766B1 (en) * 2000-01-12 2002-01-22 Transition Optical, Inc. Substituted napthopyrans
EP1461330B1 (de) * 2002-01-03 2008-03-12 Rodenstock GmbH 3H-NAPHTHO[2,1-b]-PYRAN-DERIVATE SOWIE DEREN VERWENDUNG
US7169941B2 (en) 2002-05-22 2007-01-30 Tokuyama Corporation Photochromic composition
DE60311622T2 (de) * 2002-10-18 2007-10-25 L'oreal Kosmetische Zusammensetzung enthaltend eine Ölphase und einen Farbstoff aus der Gruppe der Naphthopyrane sowie Methode
DE60318365T2 (de) * 2002-10-18 2008-12-18 L'oreal Kosmetische Zusammensetzung enthaltend mindestens zwei Farbstoffe wobei mindestens einer derselben Photochromizität aufweist
US20040228817A1 (en) * 2002-10-18 2004-11-18 L'oreal Makeup combining at least one photochromic dye and at least one goniochromatic agent
US20040228818A1 (en) * 2002-10-18 2004-11-18 L'oreal Cosmetic composition combining at least two dyes including at least one photochromic dye
EP1410785B1 (fr) * 2002-10-18 2007-01-03 L'oreal Produit de maquillage associant deux compositions à base respectivement d'une matière colorante photochrome et d'un agent goniochromatique
US20050276767A1 (en) * 2002-10-18 2005-12-15 L'oreal Composition containing an oily phase and a naphthopyran dye, cosmetic treatment processes
US8211338B2 (en) 2003-07-01 2012-07-03 Transitions Optical, Inc Photochromic compounds
US8518546B2 (en) 2003-07-01 2013-08-27 Transitions Optical, Inc. Photochromic compounds and compositions
US8545984B2 (en) 2003-07-01 2013-10-01 Transitions Optical, Inc. Photochromic compounds and compositions
US8698117B2 (en) 2003-07-01 2014-04-15 Transitions Optical, Inc. Indeno-fused ring compounds
WO2005035529A1 (de) * 2003-09-18 2005-04-21 Rodenstock Gmbh Substituierte phenanthropyrane
KR100649959B1 (ko) 2005-08-30 2006-11-27 한국화학연구원 나프토피란계 광변색 염료의 제조방법
JP2007091595A (ja) * 2005-09-27 2007-04-12 Tokuyama Corp ナフトピラン化合物の製造方法
DE102012100252A1 (de) 2011-01-26 2012-07-26 Thüringisches Institut für Textil- und Kunststoff-Forschung e.V. Polymerzusammensetzung und Verfahren zur Herstellung von Produkten mit variabler biologischer Abbaubarkeit

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8614680D0 (en) * 1986-06-17 1986-07-23 Plessey Co Plc Photoreactive lenses
GB9306587D0 (en) * 1993-03-30 1993-05-26 Pilkington Plc Photochromic compounds
US5466398A (en) * 1993-06-21 1995-11-14 Transitions Optical, Inc. Photochromic substituted naphthopyran compounds
US5384077A (en) * 1993-06-21 1995-01-24 Transitions Optical, Inc. Photochromic naphthopyran compounds
US5552090A (en) * 1993-06-21 1996-09-03 Ppg Industries, Inc. Photochromic naphthopyran compounds
JPH09124645A (ja) * 1995-11-02 1997-05-13 Tokuyama Corp クロメン化合物
AU710875B2 (en) * 1995-12-06 1999-09-30 Tokuyama Corporation Chromene compounds and photochromic materials
JP3982770B2 (ja) * 1997-04-30 2007-09-26 株式会社トクヤマ クロメン化合物
US5879592A (en) * 1997-12-10 1999-03-09 Ppg Industries, Inc. Water soluble photochromic compounds, compositions and optical elements comprising the compounds
GB9726361D0 (en) * 1997-12-12 1998-02-11 James Robinson Ltd Photochromic dyes
DE19913687A1 (de) * 1998-03-25 1999-12-02 Rodenstock Optik G Photochrome Diaryl-Naphthopyrane mit zumindest einem aminosubstituierten Arylrest

Also Published As

Publication number Publication date
DE69806367T2 (de) 2003-04-03
US6294112B1 (en) 2001-09-25
EP0973761B1 (en) 2002-07-03
DK0973761T3 (da) 2002-07-22
GB2338233A (en) 1999-12-15
GB2338233B (en) 2001-09-05
EP0973761A1 (en) 2000-01-26
JP4324661B2 (ja) 2009-09-02
JP2001518893A (ja) 2001-10-16
DE69806367D1 (de) 2002-08-08
WO1998045281A1 (en) 1998-10-15
GB9922328D0 (en) 1999-11-17
GB9706939D0 (en) 1997-05-21

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