IP Library Granted Patent US 7,208,142
Granted Patent B2
US 7,208,142 · App. 10/008,044 · Granted Apr 24, 2007

Indanylidene compounds

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,208,142
App. No.
10/008,044
Granted
Apr 24, 2007
Kind
B2
Abstract

Novel indanylidene compounds can be used as UV-A filters in cosmetic compositions for protecting skin and hair and for technical applications.

Claims (40)

1. An indanylidene compound according to the formula

2. A UV absorber mixture comprising one or more indanylidene compounds according to claim 1 .

3. A mixture comprising a UV absorber which comprises one or more indanylidene compounds according to claim 1 .

4. An indanylidene compound selected from the group consisting of 2-(5-methoxy-3,3,4,6-tetramethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(3,3,6-tetramethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(3,3,5,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5,6-ethoxylenedioxo-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5-methoxy-3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5-methyl-3,3-dimethyl-1-indanylidene) -4,4-dimethyl-3-oxo-pentanonitrile, 2-(5-methoxy-3,3-dimethyl-1-indanylidene)-4,4dimethyl -3oxo-pentanonitrile, 2-(5-t-butyl-3,3-dimethyl-1indanylidene)-4,4-dimethyl-3-oxo -pentanonitrile, 2-(5-n-butoxy-3,3,4-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo -pentanonitrile, 2-(5-n-butoxy-3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo -pentanonitrile, 2-[(5-methoxy-3,3-dimethyl-(2-methyl-3-(1,3,3,3-tetramethyl-1-(trimethyl -silyloxy)-disiloxanyl)-propyl)-indanylidene)]-4,4-dimethyl-3-oxo-pentanonitrile, and 2-(6-acetoxy-3,3-dimethyl-5-methoxy-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile.

5. A UV absorber mixture comprising a compound of the formula

in which

R 1 to R 4 independently of one another are hydrogen, C 1 –C 20 -alkyl or C 5 –C 10 cycloalkyl, with the proviso that two substituents on adjacent carbon atoms can together also be an optionally substituted C 1 –C 4 -alkylene group forming a ring;

may also, independently of one another, be C 2 –C 20 -alkyl, in which at least one methylene group may be replaced by oxygen, C 3 –C 20 -alkenyl, C 3 –C 20 -alkynyl or a group S,

where S may be a silane, an oligosiloxane or a polysiloxane group;

R 5 to R 8 , independently of one another, are hydrogen, C 1 –C 20 -alkyl or C 5 –C 10 -cycloalkyl or C 1 –C 20 -alkoxy, C 5 –C 10 -cycloalkoxy, hydroxyl, acetoxy, acetamino, carboxyl, carbalkoxy or carbamoyl,

additionally two substituents of R 5 to R 8 on adjacent carbon atoms can together form a 5–7-membered ring which contains up to three heteroatoms, where the ring atoms may be substituted by exocyclically doubled-bonded oxygen (keto group),

also, in the case of alkoxy, may, independently of one another, be C 2 –C 20 -alkyl in which at least one methylene group may be replaced by oxygen, C 3 –C 20 -alkenyl, C 3 –C 20 -alkynyl or a group S,

where S may be a silane, an oligosiloxane or a polysiloxane group;

X is cyano, CON(R) 2 or CO 2 R, where R is hydrogen or C 1 –C 8 -alkyl;

and one or more UV absorbers having a methoxycinnamate structure, a dibenzoylmethane structure, or derivatives thereof.

6. A cosmetic composition for protecting skin and hair, comprising indanylidene compounds of the formula

in which

R 1 to R 4 , independently of one another are hydrogen, C 1 –C 20 -alkyl or C 5 –C 10 -cycloalkyl, with the proviso that two substituents on adjacent carbon atoms can together also be an optionally substituted C 1 –C 4 -alkylene group forming a ring;

may also, independently of one another, be C 2 –C 20 -alkyl, in which at least one methylene group may be replaced by oxygen, C 3 –C 20 -alkenyl, C 3 –C 20 -alkynyl or a group S,

where S may be a silane, an oligosiloxane or a polysiloxane group;

R 5 to R 8 , independently of one another, are hydrogen, C 1 –C 20 -alkyl or C 5 –C 10 cycloalkyl or C 1 –C 20 -alkoxy, C 5 –C 10 -cycloalkoxy, hydroxyl, acetoxy, acetamino, carboxyl, carbalkoxy or carbamoyl,

additionally two substituents of R 5 to R 8 on adjacent carbon atoms can together form a 5–7-membered ring which contains up to three heteroatoms, in particular oxygen or nitrogen, where the ring atoms may be substituted by exocyclically doubled-bonded oxygen (keto group),

also, in the case of alkoxy, may, independently of one another, be C 2 –C 20 -alkyl in which at least one methylene group may be replaced by oxygen, C 3 –C 20 -alkenyl, C 3 –C 20 -alkynyl or a group S,

where S may be a silane, an oligosiloxane or a polysiloxane group;

X is cyano, CON(R) 2 or CO 2 R, where R is hydrogen or C 1 –C 8 -alkyl.

7. The cosmetic composition for protecting skin and hair according to claim 6 , comprising 2-(5,6-dimethoxy-3,3-dimethyl-1-indanylidene)-4,4-dimethyl -3-oxo-pentanonitrile, 2-(5-methoxy-3,3,4,6-tetramethyl -1-indanylidene)-4,4-dimethyl -3-oxo-pentanonitrile, 2-(3,3,5,6-tetramethyl-1-indanylidene)-4,4-dimethyl-3-oxo -pentanonitrile, 2-(3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5,6-ethylenedioxo-3,3dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5-methoxy-3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2[(5-methoxy-3,3-dimethyl-(2-methyl-3-(1,3,3,3-tetramethyl-1-(trimethyl-silyloxy) -disiloxanyl)-propyl)-indanylidene)]-4,4-dimethyl-3-oxo-pentanonitrile, or 2-(6-acetoxy-3,3-dimethyl-5-methoxy-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile.

8. The cosmetic composition according to claim 6 , wherein said indanylidene compound is a UV absorber and protects the skin and/or the hair against UV radiation.

9. The cosmetic composition according to claim 6 , wherein said composition further comprises at least one tanning agent and/or artificial self-tanning agent for the skin.

10. The cosmetic composition according to claim 6 , wherein said composition further comprises one or more further UV absorbers.

11. The cosmetic composition according to claim 6 , wherein said composition further comprises one or more other UV absorbers selected from the group consisting of ethylhexylmethoxy cinnamate, 2-ethylhexyl-2-cyano-3,3-diphenyl acrylate, 2-phenylbenzimidazolesulphonic acid, methylbenzylidene campher, 4-t-butyl-4′-methoxy-dibenzoylmethane, phenylene-bis-benzimidazyl-tetrasulphonic acid disodium salt, terephthalylidene-dibornanesulphonic acid and salts thereof, phenol, 2-(2H -benzotriazol-2-yl)-4-methyl-6-(2-methyl-3(1,3,3,3-tetramethyl-1-(trimethylsilyl)-oxy) -disiloxyanyl)-propyl), benzylidene malonate polysiloxane, 2,2′-methylene-bis-(6-(2H -benzotriazol-2-yl)-4-1,1,3,3-tetramethylbutyl)-phenol), 2,4-bis[{(4-(2-ethyl-hexyloxy-2-hydroxy}-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine, 4,4′,4-(1,3,5-triazine-2,4,6-triyltriimino)-tris-benzoic acid tris(2-ethylhexyl ester), 4,4′-[(6-[4-(1,1-dimethyl) -aminocarbonyl)-phenylamino]-1,3,5-triazine-2,4-diyl)diimino]-bis-(benzoic acid-2-ethylhexyl ester), zinc oxide and titanium dioxide.

12. The cosmetic composition according to claim 6 , wherein said composition further comprises UV absorbers and additionally coated or noncoated pigments or nanopigments of metal oxides.

13. The cosmetic composition according to claim 6 , wherein said composition further comprises UV absorbers and additionally finely divided pigments such that a UV broad-band protection performance with a critical wavelength λ crit >380 nm results therefrom.

14. A cosmetic composition for protecting skin and hair, comprising one or more indanylidene compounds of the formula:

15. The cosmetic composition according to claim 14 , wherein said indanylidene compounds are UV absorbers and protect the skin and/or the hair against UV radiation.

16. The cosmetic composition according to claim 14 , wherein said composition further comprises at least one tanning agent and/or artificial self-tanning agent for the skin.

17. The cosmetic composition according to claim 14 , wherein said composition further comprises one or more further UV absorbers.

18. The cosmetic composition according to claim 14 , wherein said composition further comprises one or more other UV absorbers selected from the group consisting of ethylhexylmethoxy cinnamate, 2-ethylhexyl-2-cyano-3,3-diphenyl acrylate, 2-phenylbenzimidazolesulphonic acid, methylbenzylidene campher, 4-t-butyl-4′-methoxy-dibenzoylmethane, phenylene-bis-benzimidazyl-tetrasulphonic acid disodium salt, terephthadylidene-dibornanesulphonic acid and salts thereof, phenol, 2-(2H -benzotriazol-2-yl)-4-methyl-6-(2-methyl-3(1,3,3,3-tetramethyl-1(trimethylsilyl)-oxy) -disiloxyanyl)-propyl), benzylidene malonate polysiloxane, 2,2′-methylene-bis-(6-(2H -benzotriazol-2-yl)-4-1,1,3,3-tetrmethylbutyl)-phenol), 2,4-bis[{(4-(2-ethyl-hexyloxy-2-hydroxy}-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine, 4,4′,4-(1,3,5-triazine-2,4,6-triyltriimino)-tris-benzoic acid tris(2-ethylhexyl ester), 4,4′-[(6[4-(1,1-dimethyl) -aminocarbonyl)-phenylamino]-1,3,5-triazine-2,4-diyl)diimino]-bis-(benzoic acid-2-ethylhexyl ester), zinc oxide and titanium dioxide.

19. The cosmetic composition according to claim 14 , wherein said composition further comprises UV absorbers and additionally coated or noncoated pigments or nanopigments of metal oxides.

20. The cosmetic composition according to claim 14 , wherein said composition further comprises UV absorbers and additionally finely divided pigments such that a UV broad-band protection performance with a critical wavelength λ crit >380 nm results therefrom.

21. A cosmetic composition for protecting skin and hair, comprising the indanylidene compound selected from the group consisting of 2-(5-methoxy-3,3,4,6-tetramethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(3,3,5,6-tetramethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile 2-(3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5,6-ethylenedioxo-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5-methoxy-3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5-methyl-3,3-dimethyl-1-indanylidene)-4,4-dimethyl -3-oxo-pentanonitrile, 2-(5-methoxy-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo -pentanonitrile, 2-(5-t-butyl-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo -pentanonitrile, 2-(5-n-butoxy-3,3,4-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo -pentanonitrile, 2-(5-n-butoxy-3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo -pentanonitrile, 2-[(5-methoxy-3,3-dimethyl-(2-methyl-3-(1,3,3,3-tetramethyl-1-(trimethyl-silyloxy)-disiloxanyl)-propyl)-indanylidene)]-4,4dimethyl-3-oxo-pentanonitrile, 2-(5,6-dimethoxy-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, and 2-(6-acetoxy-3,3-dimethyl-5-methoxy-1-indanylidene4,4-dimethyl-3-oxo-pentanonitrile.

Assignments (2)
MERGER AND CHANGE OF NAME Recorded Jan 20, 2004
From: HAARMANN & REIMER GMBH
To: SYMRISE GMBH & CO. KG
Reel/Frame 014895/0552 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2002
From: KOCH, OSKAR; DILK, ERICH; LANGNER, ROLAND; JOHNCOCK, WILLIAM
To: HAARMANN & REIMER GMBH
Reel/Frame 012692/0131 →