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EP0397170A1 Expired / Lapsed EP ⏱️ 0.0 years remaining

Disperse benzodifuranone dye compounds, their production and their use for dyeing or printing hydrophobic fibers

Assignee: Sumitomo Chemical Co Ltd
•
Filing: 1990-05-10
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Granted: —
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Expires: 2010-05-10
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Abstract

Abstract A heterocyclic compound of the formula, wherein A and B are each hydrogen, halogen, alkyl or alkoxy, R¹ is alkylene having upto 6 carbon atoms, X is direct linkage or divalent group such as -O-, -S- and the like, T and U are each hydrogen or alkyl, ℓ is 0 or 1 to 3, Q is 5-, 6- or 7- membered saturated or unsaturated heterocyclic residue, and Y is hydrogen, halogen, alkyl, alkoxy or or Y and B are taken together with each other to form methylene-dioxy, which is useful for dyeing or printing hydrophobic fiber materials with superior dyeability to give a dyed or printed product of a red color excellent in fastness properties, particu­larly those such as washing fastness.

Inventors

  • 👤 Jun Yamamoto
  • 👤 Yasuyoshi Ueda
  • 👤 Junichi Sekihachi
  • 👤 Yosuke Yamamoto
  • 👤 Takashi Omura

Bibliographic Details

Application Number —
Jurisdiction EP
Data Source google_patents
Last Synchronized 2026-11-06 11:04
CPC Classifications
C; C07; C07D; C07D493/00; C07D493/02; C07D493/04; C09; C09B; C09B57/00; Y; Y10; Y10S; Y10S8/00; Y10S8/92; Y10S8/922

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 198 words
A heterocyclic compound of the formula, wherein A and B are each independently a hydrogen atom, a halogen atom, a C₁ - C₄ alkyl group or a C₁ - C₄ alkoxy group, R¹ is a methylene group or a straight or branched C₂ - C₆ alkylene group unsubstituted or substituted by a hydroxy group, a C₁ - C₄ alkoxy group or a C₁ - C₄ alkylcarbonyloxy group, X is a direct linkage or a divalent group of -O-, -S-, -SO-, -SO₂-, in which R² is a hydrogen atom or a C₁ - C₄ alkyl group, in which R² is as defined above, T and U are each independently a hydrogen atom or a C₁ - C₄ alkyl group, ℓ is 0 or an integer of 1 to 3, Q is an unsubstituted or substituted 5-, 6- or 7-membered saturated or unsaturated heterocyclic residue, and Y is a hydrogen atoms a halogen atom, a C₁ - C₄ alkyl group, a C₁ - C₄ alkoxy group or a group of the formula in which R¹, X, T, U, ℓ and Q are as defined above, or Y and B are taken together with each other to form a methylenedioxy group.
Claim 2
Dependent Claim 198 words
A heterocyclic compound of the formula, wherein A and B are each independently a hydrogen atom, a halogen atom, a C₁ - C₄ alkyl group or a C₁ - C₄ alkoxy group, R¹ is a methylene group or a straight or branched C₂ - C₆ alkylene group unsubstituted or substituted by a hydroxy group, a C₁ - C₄ alkoxy group or a C₁ - C₄ alkylcarbonyloxy group, X is a direct linkage or a divalent group of -O-, -S-, -SO-, -SO₂-, in which R² is a hydrogen atom or a C₁ - C₄ alkyl group, in which R² is as defined above, T and U are each independently a hydrogen atom or a C₁ - C₄ alkyl group, ℓ is 0 or an integer of 1 to 3, Q is an unsubstituted or substituted 5-, 6- or 7-membered saturated or unsaturated heterocyclic residue, and Y is a hydrogen atoms a halogen atom, a C₁ - C₄ alkyl group, a C₁ - C₄ alkoxy group or a group of the formula in which R¹, X, T, U, ℓ and Q are as defined above, or Y and B are taken together with each other to form a methylenedioxy group.
Claim 3
Dependent Claim 78 words
The compound according to Claim 1, wherein Q is a 5-, 6- or 7-membered unsaturated heterocyclic residue unsubstituted or substituted once or twice by a halogen atom, a hydroxy group, a C₁ - C₄ alkyl group, a C₁ - C₄ alkoxy group, a C₁ - C₄ alkylcarbonyl group, a C₁ - C₄ alkoxycarbonyl group, a cyano group, a keto group or a primary, secondary or tertiary amino group unsubstituted or substituted by a C₁ - C₄ alkyl group.
Claim 4
Dependent Claim 29 words
The compound according to Claim 2, wherein the heterocyclic residue is furyl, thienyl, pyrrolyl, pyridyl, pyranyl, thiazolyl, oxazolyl, pyrazolyl, imidazolyl, thiadiazolyl, s-triazinyl, benzofuranyl, benzothienyl, indolyl, benzoxazolyl, benzimidazolyl or benzothiazolyl.
Claim 5
Dependent Claim 78 words
The compound according to Claim 1, wherein Q is a 5-, 6- or 7-membered saturated heterocyclic residue unsubstituted or substituted once or twice by a halogen atom, a hydroxy group, a C₁ - C₄ alkyl group, a C₁ - C₄ alkoxy group, a C₁ - C₄ alkyl­carbonyl group, a C₁ - C₄ alkoxycarbonyl group, a cyano group, a keto group or a primary, secondary or tertiary amino group unsubstituted or substituted by a C₁ - C₄ alkyl group.
Claim 6
Dependent Claim 21 words
The compound according to Claim 4, wherein the saturated heterocyclic residue is tetrahydro­furyl, tetrahydrothienyl, pyrrolidyl, piperidyl, tetrahydropyranyl, piperazinyl, morpholinyl or hexahydroazepinyl.
Claim 7
Dependent Claim 29 words
The compound according to Claim 5, werein the saturated heterocyclic residue is 2-tetrahydro­ furyl, tetrahydropyranyl, piperidyl, pyrrolidyl or morpholinyl unsubstituted or substituted by a C₁ - C₄ alkyl group.
Claim 8
Dependent Claim 10 words
The compound according to Claim 1, wherein ℓ is 0.
Claim 9
Dependent Claim 14 words
The compound according to Claim 1, wherein A, B and Y are hydrogen atoms.
Claim 10
Dependent Claim 20 words
The compound according to Claim 1, where R¹ is a methylene group or a straight C₂ - C₄ alkylene group.
Claim 11
Dependent Claim 55 words
A process for producing the heterocyclic compound according to Claim 1, which comprises reacting a mandelic acid of the following formula (II), wherein A, R¹, X, T, U, ℓ and Q are as defined in Claim 1, with a compound of the following formula (III), wherein B and Y are as defined in Claim 1.
Claim 12
Dependent Claim 23 words
A process for dyeing or printing hydro­phobic fiber materials, which comprises contacting the fiber materials with the heterocyclic compound according to Claim 1.
Claim 13
Dependent Claim 13 words
Hydrophobic fiber materials dyed or printed by the process according the Claim 11.
Claim 14
Dependent Claim 13 words
Use of the heterocyclic compound according to Claim 1 as a disperse dye.

References Cited (Backward Citations)

EP0033583A1 Cited
GB2103231A Cited
EP0146269A2 Cited
EP0182507A2 Cited

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