IP Library Granted Patent US 12,227,898
Granted Patent B2
US 12,227,898 · App. 18/372,893 · Granted Feb 18, 2025

Pyridine and pyrimidine substituted triazine UV absorbers

Inventors: Hosuk Ryu (Arlesheim, CH); Hans-Jorg Peter (Basel, CH); Gilles Sperissen (Eschentzwiller, FR); Martin Weber (Steinen, DE)
Assignee: Archroma (Switzerland) GmbH
D06P5/06C07D401/04C07D403/04C09K15/30D06M13/358D06P1/445D06P1/6426D06P3/52D06M2101/32D06M2200/25
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Quick Facts
Patent No.
US 12,227,898
App. No.
18/372,893
Granted
Feb 18, 2025
Kind
B2
Abstract

A compound of formula wherein V, W, X and Y represent N or CH, at least one of V, W, X and Y being N and at least two of V, W, X and Y being CH; R 1 , R 2 and R 3 are each independently of the other hydrogen, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, nitro, cyano, trifluoromethyl, halogen or hydroxy; and the compound provides good lightfastness properties to textile fibre materials, in particular PES fibre materials.

Claims (52)

1. A compound of formula

wherein V, X and Y represent N or CH, one or two of V, X and Y being N and the remainder of V, X and Y being CH;

W is CH; and

R 1 , R 2 and R 3 are each independently of the other hydrogen, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, nitro, cyano, trifluoromethyl, halogen or hydroxy;

with the proviso that the compounds of formulae

are excluded.

2. The compound of formula (1) according to claim 1 , wherein

X is N; and

V and Y are CH.

3. The compound of formula (1) according to claim 1 , wherein

Y is N; and

V and X are CH.

4. The compound of formula (1) according to claim 1 , wherein

V is N; and

W and Y are CH.

5. The compound of formula (1) according to claim 1 , wherein R 1 is hydrogen, methyl or methoxy.

6. The compound of formula (1) according to claim 1 , wherein R 1 is hydrogen or methoxy.

7. The compound of formula (1) according to claim 1 , wherein R 2 is hydrogen, methyl, methoxy, nitro, cyano, trifluoromethyl, halogen or hydroxy.

8. The compound of formula (1) according to claim 1 , wherein R 2 is hydrogen or methoxy.

9. The compound of formula (1) according to claim 1 , wherein R 3 is hydrogen, methyl, methoxy, nitro, cyano, trifluoromethyl, halogen or hydroxy.

10. The compound of formula (1) according to claim 1 , wherein R 3 is hydrogen or methoxy.

11. The compound of formula (1) according to claim 1 , wherein the C 1 -C 8 alkyl is methyl and the C 1 -C 8 alkoxy is methoxy.

12. A photochemically stabilized textile fiber material comprising undyed, dyed or printed textile fiber material and at least one compound of formula

wherein

V, X and Y represent N or CH, one or two of V, X and Y being N and the remainder of V, X and Y being CH;

W is CH; and

R 1 , R 2 and R 3 are each independently of the other hydrogen, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, nitro, cyano, trifluoromethyl, halogen or hydroxy;

with the proviso that the compounds of formulae

are excluded.

13. The photochemically stabilized textile fiber material of claim 12 wherein R 1 , R 2 and R 3 are each independently hydrogen or methoxy.

14. The photochemically stabilized textile fiber material of claim 12 wherein the undyed, dyed or printed textile fiber material comprises polyester fibers.

15. The photochemically stabilized textile fiber material of claim 12 comprising from 0.01% to 15.0% by weight of the compound of formula (1).

16. A process for the photochemical stabilization of textile fiber material, comprising treating an undyed, dyed or printed textile fiber material with a liquor comprising at least one compound of formula

wherein

V, X and Y represent N or CH, one or two of V, X and Y being N and the remainder of V, X and Y being CH;

W is CH; and

R 1 , R 2 and R 3 are each independently of the other hydrogen, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, nitro, cyano, trifluoromethyl, halogen or hydroxy;

with the proviso that the compounds of formulae

are excluded.

17. The process of claim 16 wherein R 1 , R 2 and R 3 are each independently hydrogen or methoxy.

18. The process of claim 16 wherein the undyed, dyed or printed textile fibre material comprises polyester fibres.

19. A process for the preparation of a compound of formula (1), comprising

(I) preparing 2-aryl-4H-1,3-benzoxazin-4-one (4) by acid-catalysed ring closure reaction of salicylamide derivative (2) with carboxylic acid (3)

and

(II) reacting the 2-aryl-4H-1,3-benzoxazin-4-one (4) with amidine (5) to provide the compound of formula (1)

wherein

V, X and Y represent N or CH, one or two of V, X and Y being N and the remainder of V, X and Y being CH;

W is CH; and

R 1 , R 2 and R 3 are each independently of the other hydrogen, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, nitro, cyano, trifluoromethyl, halogen or hydroxy;

with the proviso that the compounds of formulae

are excluded.

20. The process of claim 19 wherein R 1 , R 2 and R 3 are each independently hydrogen or methoxy.

Assignments (3)
CHANGE OF NAME Recorded Dec 3, 2024
From: HUNTSMAN TEXTILE EFFECTS (SWITZERLAND) GMBH
To: ARCHROMA (SWITZERLAND) GMBH
Reel/Frame 069473/0963 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2024
From: RYU, HOSUK; PETER, HANS-JÖRG; SPERISSEN, GILLES; WEBER, MARTIN
To: HUNTSMAN ADVANCED MATERIALS (SWITZERLAND) GMBH
Reel/Frame 069093/0347 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2024
From: HUNTSMAN ADVANCED MATERIALS (SWITZERLAND) GMBH
To: HUNTSMAN TEXTILE EFFECTS (SWITZERLAND) GMBH
Reel/Frame 069095/0414 →
Priority Claims (1)
EP 18198408 · Sep 26, 2023 · regional
Continuity (2)
Continuation 17280944
Related Publication 20240102236A1 · Mar 28, 2024
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