IP Library Granted Patent US 7,074,943
Granted Patent B2
US 7,074,943 · App. 11/242,199 · Granted Jul 11, 2006

Oxygen-containing heterocyclic fused naphthopyrans

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Quick Facts
Patent No.
US 7,074,943
App. No.
11/242,199
Granted
Jul 11, 2006
Kind
B2
Abstract

This invention relates to novel naphthopyrans having an oxygen-containing heterocyclic group F annelated on the i, j, or k side of the naphthopyran ring, having certain substituents at the 2, 5, and 6 positions of the naphthopyran ring. These naphthopyrans may have the formula (I) presented below: These compounds (I) have interesting photochromic properties. Also related to this invention are host materials that contain such naphthopyran compounds, and articles such as ophthalmic lenses or other plastic transparencies that incorporate the naphthopyran compounds.

Claims (107)

1. A naphthopyran compound of the following formula:

wherein

(a) F is a 5- to 7-member saturated heterocyclic ring group fused to i side of the naphthopyran ring and containing an oxygen atom at the position adjacent to position 7-, or 8-position;

(b) R 6 represents

a hydrogen,

a C1–C6 alkyl, alkoxy,

a —C(O)R group, wherein R is selected from hydrogen, hydroxy, alkyl, alkoxy,

an aryl or heteroaryl group which is in its basic structure (that is, in its ring atoms, the rings have 5, 6 or 7 atoms) 6 to 24 carbon atoms or 4 to 24 carbon atoms respectively and at least one heteroatom selected from sulfur, oxygen and nitrogen; the basic structure being optionally substituted with at least one substituent selected from:

a halogen atom (e.g., fluorine, chlorine and bromine),

a hydroxy group,

a linear or branched alkyl group consisting of 1 to 12 carbon atoms,

a linear or branched alkoxy group consisting of 1 to 12 carbon atoms,

a haloalkyl or haloalkoxy group corresponding to the (C1–C12) alkyl or alkoxy groups above respectively which are substituted with at least one halogen atom, and notably a fluoroalkyl group of this type,

a linear or branched alkenyl group consisting of 2 to 12 carbon atoms, and notably a vinyl group or an allyl group,

an —NH 2 group,

an —NHR 8 group, R 8 representing a linear or branched alkyl group consisting of 1 to 6 carbon atoms,

a

group, in which R 9 and R 10 , which are the same or different, independently representing a linear or branched alkyl group consisting of 1 to 6 carbon atoms, or representing (together with the nitrogen atom to which they are bound) a 5- to 7-membered ring which consists of at least one other heteroatom selected from oxygen, sulfur and nitrogen, said nitrogen being optionally substituted with a group that is a linear or branched alkyl group consisting of 1 to 6 carbon atoms,

a methacryloyl group or an acryloyl group,

a polyether, polyamide, polycarbonate, polycarbamate, polyurea or polyester residue;

(c) R 5 represents:

a hydroxy,

a halogen, and notably fluorine, chlorine or bromine,

a linear or branched alkyl group which consists of 1 to 12 carbon atoms (advantageously 1 to 6 carbon atoms),

a cycloalkyl group consisting of 3 to 12 carbon atoms,

a linear or branched alkoxy group consisting of 1 to 12 carbon atoms (most advantageously 1 to 6 carbon atoms),

a haloalkyl, halocycloalkyl, or haloalkoxy group corresponding to the alkyl, cycloalkyl, alkoxy groups above respectively, which are substituted with at least one halogen atom, notably selected from fluorine, chlorine and bromine,

a linear or branched alkenyl or alkynyl group consisting of 1–12 carbon atoms, preferably a vinyl or allyl group,

a linear or branched alkenyloxy or alkynyloxy group consisting 1–12 carbon atoms, preferably an allyloxy group,

an aryl or heteroaryl group having the same definition as R 6 given supra,

an aralkyl or heteroaralkyl group, the alkyl group, which is linear or branched, consisting of 1 to 4 carbon atoms, and the aryl and heteroaryl groups having the same definitions as R6 given supra,

an amine or amide group: —NH 2 , —NHR 8 , —CONH 2 , —CONHR 8 ,

R 8 , R 9 , and R 10 having their respective definitions given above for the amine substituents of the values R 6 ,

a —C(R 11 ) 2 X group, wherein X is —CN, halogen, hydroxy, alkoxy, benzoyloxy, C1–C6 acyloxy, amino, C1–C6 mono-alklamino, C1–C6 dialkyl amino, morpholino, piperidino, 1-indolinyl, pyrrolidyl, or trimethylsilyloxy, R 16 is hydrogen, C1–C6 alkyl, phenyl or naphthyl with C1–C6 alkyl or C1–C6 alkoxy substituents,

an —OCOR 12 or —COOR 12 group, R 12 representing a straight or branched alkyl group consisting of 1 to 6 carbon atoms, or a cycloalkyl group consisting of 3 to 7 carbon atoms, or a phenyl group, optionally substituted with at least one of the substituents listed above within the values in the definitions of R 6 ,

a methacryloyl group or an acryloyl group, an epoxy group having the formula,

in which k=1, 2 or 3,

a polyether, polyamide, polycarbonate, polycarbamate, polyurea or polyester residue;

(d) R 1 and R 2 , which are identical or different, independently represent:

a hydrogen,

a linear or branched alkyl group which consists of 1 to 12 carbon atoms (with or without substitution),

a cycloalkyl group which consists of 3 to 12 carbon atoms,

an aryl or heteroaryl group as R 6 defined supra,

an aralkyl or heteroaralkyl group, the alkyl group, which is linear or branched, consisting of 1 to 4 carbon atoms and the aryl and heteroaryl groups having the definitions given above, or

the two substituents R 1 and R 2 together forming a ring selected from the group consisting of an adamantyl, norbornyl, fluorenylidene, 5,5- or 10,10-di(C1–C6)alkylanthracenylidene, 5 (or 10)-(C1–C6)alkyl-5 (or 10)-OH (or OR 15 )anthracenylidene or spiro(C5–C6)cycloalkylanthracenylidene ring group; said ring group being optionally substituted with at least one of the substituents listed above in the definitions for R 1 , R 2 ; said ring group being optionally substituted with two adjacent groups that form a 5- to 6-member aromatic or non-aromatic ring which can have at least one heteroatom selected from oxygen, sulfur, and nitrogen;

(e) each R 7 group can be the same or different, independently representing

a hydrogen,

a linear, branched, or cyclic alkyl group,

a linear, branched, or cyclic alkoxy group,

a linear or branched alkenyl or alkynyl group,

a linear or branched alkenyloxy or alkynyloxy group,

an aryl or heteroaryl group having the same definition as that given supra for R 6 ,

two of the R 7 groups, which are adjacent or bonded to the same carbon atom in the group F, form a 5- to 7-membered non-aromatic ring which consists of at least one hetroatom selected from the group consisting of oxygen, sulfur, and nitrogen, and

m is an integer of 0 to 6.

2. The naphthopyran compound according to claim 1 , wherein:

m is an integer of 1 or 2,

R′ 1 and R′ 2 , same or different, represent

a hydrogen,

a linear, branched, or cyclic alkyl,

an alkyoxy with the alkyl portion being linear, branched, or cyclic,

an unsubstituted, mono- or di-substituted aromatic group,

an aryloxy with the aryl being unsubstituted, mono- or di-substituted;

R 5 represents

a linear, branched, or cyclic alkyl group,

a linear or branched alkenyl or alkynyl group,

a —C(R 11 ) 2 X group, wherein X is hydroxy, alkoxy, benzoyloxy, C1–C6 acyloxy,

an optionally substituted phenyl or benzyl group,

a —COR 12 , or —COOR 12 group, R 12 representing a linear, branched, or cyclic alkyl group consisting of 1 to 6 carbon atoms;

R 6 represents a unsubstituted, mono- or di-substituted aromatic or hetero-aromatic group selected from phenyl, naphthyl, pyridyl, furanyl, benzofuranyl, thenyl, benzothienyl;

R 7 represents

a hydrogen,

a linear, branched, or cyclic alkyl group,

a linear, branched, or cyclic alkoxy group,

a linear or branched alkenyl or alkynyl group,

a linear or branched alkenyloxy or alkynyloxy group,

an aryl or heteroaryl group having the same definition as that given supra for R 6 ,

two of the R 7 groups, which are adjacent or bonded to the same carbon atom in the group F, form a 5- to 7-membered non-aromatic ring which consists of at least one hetroatom selected from the group consisting of oxygen, sulfur, and nitrogen, and

m is an integer of 0 to 2.

3. The naphthopyran compound according to claim 1 , being further crosslinked.

4. The naphthopyran compound according to claim 1 , being further polymerized.

5. A photochromic composition comprising:

at least one compound according to claim 1 ;

at least one linear or cross-linked (co)polymer which contains, in its structure, at least one compound according to claim 1 ;

at least one additional photochromic compound of another type;

at least one non-photochromic coloring agent; and

at least one stabilizing agent.

6. The naphthopyran compound according to claim 1 being further incorporated into a (co)polymer matrix.

7. The naphthopyran composition according to claim 5 being further incorporated into a (co)polymer matrix.

8. A (co)polymer matrix comprising at least one co(polymer) and/or reticulate according to claim 4 .

9. A (co)polymer matrix according to claim 6 further comprising one or more (co)polymer selected from the group consisting of: an alkyl, cycloalkyl, (poly or oligo)ethylene glycol or aryl or arylalkyl mono-, di-, tri-, or tetraacrylate or mono-, di-, tri-, or tetramethacrylate which is optionally halogenated or which optionally comprises at least one ether and/or ester and/or carbonate and/or carbamate and/or thiocarbamate and/or urea and/or amide group; polystyrene, polyether, polyester, polycarbonate, polycarbamate, polyepoxy, polyurea, polyurethane, polythiourethane, polysiloxane, polyacrylonitrile, polyamide, aliphatic or aromatic polyester, vinylic polymers, cellulose acetate, cellulose triacetate, cellulose acetate-propionate, polyvinylbutyral, poly(methyl methacrylate), poly(ethylene glycol bismethacrylate), poly(ethoxylated bisphenol A dimethacrylate), poly(vinyl acetate), polyvinylbutyral, polyurethane, polyanhydride and polymers of members of the group consisting of diethylene glycol bis(allyl carbonate) monomers, diethylene glycol dimethacrylate monomers, ethoxylated phenol bismethacrylate monomers, diisopropenyl benzene monomers and ethoxylated trimethylol propane triacrylate monomers.

10. The naphthopyran compound according to claim 1 being further incorporated into an ophthalmic lens.

11. The naphthopyran composition according to claim 5 being further incorporated into an ophthalmic lens.

12. The naphthopyran compound according to claim 3 being further incorporated into an ophthalmic lens.

13. The naphthopyran (co)polymer matrix according to claim 6 being further incorporated into an ophthalmic lens.

14. The naphthopyran (co)polymer matrix according to claim 9 being further incorporated into an ophthalmic lens.

15. A naphthopyran compound of the following formula:

in which,

R′ 1 , R′ 2 and R′ 6 , same or different, represent

a linear, branched, or cyclic alkyl group,

an alkyoxy group with the alkyl portion being linear, branched, or cyclic;

R 5 represents

a linear, branched, or cyclic alkyl group,

an linear or branched alkenyl or alkynyl group,

a —C(R 11 ) 2 X group, wherein X is hydroxy, alkoxy, benzoyloxy, C1–C6 acyloxy, R 11 is hydrogen or C1–C6 alkyl,

a substituted phenyl or benzyl group,

a —COR 12 , or —COOR 12 group, R 12 representing a linear, branched, or

cyclic alkyl group having 1 to 6 carbon atoms, or an substituted phenyl or benzyl group.

Assignments (13)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2022
From: VISION EASE, LP
To: HOYA OPTICAL LABS OF AMERICA, INC.
Reel/Frame 059825/0497 →
RELEASE OF SECURITY INTEREST Recorded Aug 1, 2017
From: ANTARES CAPITAL LP
To: VISION EASE, LP
Reel/Frame 043402/0306 →
CHANGE OF NAME Recorded Nov 23, 2015
From: INSIGHT EQUITY A.P. X, LP
To: VISION EASE, LP
Reel/Frame 037154/0842 →
RELEASE OF SECURITY INTEREST Recorded Oct 30, 2015
From: ANTARES CAPITAL LP, AS AGENT
To: VISION EASE, LP (F/N/A INSIGHT EQUITY A.P. X, LP)
Reel/Frame 037009/0180 →
SECURITY INTEREST Recorded Oct 27, 2015
From: VISION EASE, LP (D/B/A VISION-EASE LENS)
To: ANTARES CAPITAL LP, AS ADMINISTRATIVE AGENT
Reel/Frame 036981/0268 →
ASSIGNMENT OF INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Sep 15, 2015
From: GENERAL ELECTRIC CAPITAL CORPORATION, AS RETIRING AGENT
To: ANTARES CAPITAL LP, AS SUCCESSOR AGENT
Reel/Frame 036616/0161 →
RELEASE OF SECURITY INTEREST Recorded Sep 23, 2014
From: PNC BANK, NATIONAL ASSOCIATION, AS REVOLVING AGENT
To: INSIGHT EQUITY A.P. X, LP
Reel/Frame 033810/0185 →
RELEASE OF SECURITY INTEREST Recorded Sep 23, 2014
From: PNC BANK, NATIONAL ASSOCIATION, AS TERM LOAN AGENT
To: INSIGHT EQUITY A.P. X, LP
Reel/Frame 033810/0143 →
SECURITY INTEREST Recorded Sep 23, 2014
From: INSIGHT EQUITY A.P. X, LP (D/B/A VISION-EASE LENS)
To: GENERAL ELECTRIC CAPITAL CORPORATION, AS AGENT
Reel/Frame 033810/0209 →
SECURITY AGREEMENT Recorded Nov 8, 2012
From: INSIGHT EQUITY A.P. X, LP (D/B/A VISION-EASE LENS)
To: PNC BANK, NATIONAL ASSOCIATION, AS REVOLVING AGENT
Reel/Frame 029261/0832 →
SECURITY AGREEMENT Recorded Nov 8, 2012
From: INSIGHT EQUITY A.P. X, LP (D/B/A VISION-EASE LENS)
To: PNC BANK, NATIONAL ASSOCIATION, AS TERM LOAN AGENT
Reel/Frame 029261/0912 →
RELEASE OF SECURITY INTEREST Recorded Oct 30, 2012
From: ORIX CORPORATE CAPITAL INC. (F/K/A ORIX FINANCE CORP.)
To: INSIGHT EQUITY A.P. X, LP
Reel/Frame 029209/0771 →
RELEASE OF SECURITY INTEREST Recorded Oct 30, 2012
From: REGIMENT CAPITAL SPECIAL SITUATIONS FUND IV, L.P.
To: INSIGHT EQUITY A.P. X, LP
Reel/Frame 029209/0926 →