IP Library Granted Patent US 6,881,850
Granted Patent B2
US 6,881,850 · App. 10/720,442 · Granted Apr 19, 2005

Heterocyclically annellated indenochromene derivatives

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Quick Facts
Patent No.
US 6,881,850
App. No.
10/720,442
Granted
Apr 19, 2005
Kind
B2
Abstract

The present invention relates to specific photochromic heterocyclically annellated indenochromene derivatives and the use thereof in plastics of all types, particularly for ophthalmic applications. In particular, the present invention relates to indeno[1,2-h]chromene derivatives having the following general formula (I) and indeno[2,1-f]chromene derivatives having the following general formula (II):

Claims (25)

1. A photochromic indenochromene compound corresponding to formula (II):

wherein

R 1 and R 2 represent radicals independently selected from the group A, consisting of hydrogen, fluorine, chlorine, bromine, hydroxy, (C 1 -C 6 )-alkyl, (C 1 -C 6 -alkoxy, (C 2 -C 7 )-cycloaLkyl which may include one or more heteroatoms, (C 1 -C 6 )-acyl, unsubstituted or monosubstituted phenyl, and unsubstituted or monosubstituted benzyl, wherein the phenyl or benzyl substituents are selected from the group consisting of (C 1 -C 6 )-alkyl and (C 1 -C 6 )-alkcoxy; or

R 1 and H 2 together represent; an annellated, unsubstituted, monosubstituted or disubstituted benzo or pyrido ring wherein the ring substituents are selected from group A;

R 3 represents a substituent selected from the group consisting of hydrogen, (C 1 -C 6 )-alkyl, and —OM, wherein M is a substituent selected from group A;

R 4 is a substituent selected from the group consisting of hydrogen, hydroxy, (C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkaxy, (C 3 -C 7 )-cycloalkyl, (C 1 -C 6 )-acyl; unsubstituted, monosubstituted, disubstituted or trisubstituted phenyl, benzyl, naphthyl, phenanthryl, pyrenyl, quinolyl, isoquinolyl, benzofuranyl, thienyl, benzothienyl, dibenzofuranyl, dibenzothienyl, carbazolyl and indolyl, wherein the substituents are selected from group A; (C 1 -C 6 )-4-phenylalkyl and (C 1 -C 6 )-4-phenoxyalkyl, wherein the phenyl ring in 4-position in turn may be part of an additional photochromic pyran system; or

R a and R 4 together with the spiro carbon atom represent a saturated and/or unsaturated ring with 5 to 8 carbon atoms, of which at most one may be substituted by a heteroatom selected from the group consisting of O, S and NR 5 , wherein R 6 is selected from group A, and wherein at least one aromatic or heteroaromatic ring system selected from group E consisting of benzene, naphthalene, phenanthrene, pyridine, quinoline, furan, thiophene, pyrrole, benzofuran, benzothiophene, indole and carbazole, is annellated to the ring, wherein said ring system may have one or more substituents selected from group A;

the annellated ring (Het) represents a 5 or 6-member heteroaromatic ring corresponding to one of the following formulas:

wherein Y is selected from the group consisting of oxygen, sulfur and NR 5 , and Z, U, V and W are each independently selected from the group consisting of nitrogen and CR 5 , wherein R 6 and R 7 represent substituents independently selected from group A, or

R 6 and R 7 if they are ortho to one another together represent an unsubstituted or monosubstituted benzene ring wherein the ring substituents are independently selected from group A; and

B and B′ are each independently selected from the following groups a), b), c) or d); wherein

group a) consists of monosubstituted, disubstituted and trisubstituted aryl selected from the group consisting of phenyl and naphthyl;

group b) consists of unsubstituted, monosubstituted and disubstituted heteroaryl selected from the group consisting of pyridyl, furanyl, benzofuran-2-yl, benzofuran-3-yl, thien-2-yl, thien-3-yl, benzothien-2-yl, benzothien-3-yl, phenazinyl, phenoxazinyl, phenothiazinyl and julolidinyl,

wherein the substituents of the aryl or heteroaryl in groups a) and b) are selected from the group consisting of the above-defined group A, amino, mono-(C 1 -C 6 )-alkylamino, di-(C 1 -C 6 )-alkylamino, monophenylamino and diphenylamino unsubstituted, monosubstituted or disubstituted on the phenyl rings, wherein the phenyl ring substituents in turn are selected from group A, pyrrolidinyl, piperidinyl, morpholinyl, thiomorpholinyl, phenazinyl, phenoxazinyl, phenothiazinyl, carbazolyl, unsubstituted, monosubstituted and disubstituted pyrryl, wherein the pyrryl substituents are selected from group A,

group c) consists of structural units with the following structural formulas (B) and (C):

 wherein

D and E are independently selected from the group consisting of oxygen, sulfur, carbon or NR 8 ;

R 8 , R 9 , R 10 and R 11 are each independently selected from the group A; and n is 1,2, or 3;

 provided that if D represents NR 8 in formula (B), E represent; carbon, or

d) B and B′ together form an unsubstituted, monosubstituted or disubstituted fluorene-9-ylidene group or a saturated hydrocarbon group, which is C 3 -C 12 spiro monocyclic, C 7 -C 12 spiro bicyclic or C 7 -C 12 spiro tricyclic, wherein the fluorene substituents are selected from group A.

2. A photochromic indenochromene compound according to claim 1 , wherein the annellated heterocycle (Het) is selected from the group consisting of indole, benzofuryl, benzothienyl, thienyl, furyl, oxazolyl, imidazolyl, pyrimidinyl, pyrazinyl and triazinyl.

3. A photochromic indenochromene compound according to claim 1 , wherein B and B′ are each independently selected from monosubstituted, disubstituted or trisubstituted phenyl groups, wherein the phenyl group substituents are selected from the group consisting of group A, amino, mono-(C 1 -C 6 )-alkylamino, di-(C 1 -C 6 )-alkylamino, monophenyl- and diphenylamino unsubstituted, monosubstituted or disubstituted on the phenyl ring; wherein the phenyl, ring substituents in turn are selected from group A, pyrrolidinyl, piperidinyl, morpholinyl, thiomorpholinyl, phenazinyl, phenoxazinyl, phenothiazinyl, carbazolyl, unsubstituted, monosubstituted and disubstituted pyrryl, wherein the pyrryl substituents are selected from group A.

4. A photochromic indenochromene compound according to claim 1 , wherein B and B′ each independently represent a julolidinyl group.

5. A photochromic article comprising a synthetic resin body and at least one photochromic indenochromene compound according to claim 1 .

6. A photochromic article according to claim 5 , wherein said synthetic resin body is an ophthalmic lens.

Assignments (4)
CHANGE OF NAME Recorded Dec 7, 2005
From: SECOND OPTICAL HOLDING GMBH
To: RODENSTOCK GMBH
Reel/Frame 017286/0744 →
MERGER Recorded Dec 7, 2005
From: RODENSTOCK GMBH
To: SECOND OPTICAL HOLDING GMBH
Reel/Frame 017286/0756 →
MERGER Recorded Nov 24, 2004
From: RODENSTOCK GMBH
To: RODIS INFORMATIONSSYSTEME GMBH
Reel/Frame 016026/0097 →
CHANGE OF NAME Recorded Nov 24, 2004
From: RODIS INFORMATIONSSYSTEME GMBH
To: RODENSTOCK GMBH
Reel/Frame 016026/0120 →