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US4374767A Expired / Lapsed US ⏱️ 0.0 years remaining

Substituted ether or thioether isothiazole azo dyes

Assignee: Novartis Corp
•
Filing: 1980-08-11
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Granted: 1983-02-22
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Expires: 2000-08-11
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Abstract

Abstract Disclosed are novel azo dyes containing an isothiazole moiety substituted with ether or thioether groups. The dyes produce orange to violet shades on hydrophobic texture fiber including polyesters, polyamides, and cellulose esters and have excellent fastness properties including lightfastness, washfastness and resistance to sublimation. The dyes have the general formula ##STR1## R is lower alkyl or phenyl; X is O or S; R 1 is lower alkyl or substituted lower alkyl, cyclohexyl, phenyl or substituted phenyl; and when X is S, R 1 can be various heterocycles such as pyridyl, pryimidinyl, benzothiazolyl, benzoxazolyl, benzimidazolyl and azolyl radicals; R 2 is hydrogen, lower alkyl, lower alkoxy, or acylamido; R 3 is H, lower alkyl, or lower alkoxy; and R 4 and R 5 are selected from 1 to 2 of H, alkyl of 1-8 carbons, substituted alkyls, cyclohexyl, phenyl or substituted phenyl.

Inventors

  • 👤 Max A. Weaver
  • 👤 Jean C. Fleischer

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 16:28
CPC Classifications
C; C09; C09B; C09B43/00; C09B43/40; C09B29/00; C09B29/0025; C09B29/0074; C09B29/0077; C09B29/0081; C09B29/06; C09B29/08; C09B29/0805; C09B29/0807

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 241 words
Azo compounds of the formula: ##STR32## wherein R is lower alkyl or phenyl; X is O or S; R 1 is selected from lower alkyl, cyclohexyl, and phenyl wherein said lower alkyl is unsubstituted or substituted with 1-3 of --OH, Cl, Br, aryl, aryloxy, lower alkanoyloxy, lower alkoxy, or lower alkoxy substituted with --OH, Cl, Br, or lower alkoxy, and wherein said phenyl is unsubstituted or substituted with Cl, Br, lower alkoxy, or lower alkyl, and when X is S, R 1 is further selected from pyridyl, pryimidinyl, benzothiazolyl, benzoxazolyl, benzimidazolyl, azolyl radicals having the formula ##STR33## wherein Y is an oxygen or sulfur atom and Z is an ethylenically unsaturated group of two carbon atoms or of a nitrogen and a carbon atom, wherein said azolyl radicals may be substituted with lower alkyl, phenyl, or phenyl substituted as above for R 1 ; R 2 is selected from hydrogen, lower alkyl, lower alkoxy, formamido, lower alkoxycarbonylamino, lower alkanoylamino, lower alkanoylamino substituted with cyano, lower alkoxy, lower alkoxycarbonyl, phenoxy, or phenyl, phenoxy, halogen substituted phenoxy, cycloalkylcarbonyl, and lower alkylsulfonyl; R 3 is H, or lower alkyl; and R 4 and R 5 are independently selected from H, alkyl of 1-8 carbons, cyclohexyl, phenyl, lower alkoxycarbonyl substituted phenyl, and lower alkyl substituted with cyclohexyl, lower alkanoyloxy, lower alkoxycarbonyl, succinimido, lower alkanoylamino, lower alkylsulfonylamino, lower alkyl sulfonyl, sulfamoyl, carbamoyl, hydroxy, pyrrolidono, phthalimido, aryl, cyano, aryloxy, lower alkoxycarbonyloxy, lower alkoxy, phenoxy, or lower alkoxyalkoxy.
Claim 2
Dependent Claim 241 words
Azo compounds of the formula: ##STR32## wherein R is lower alkyl or phenyl; X is O or S; R 1 is selected from lower alkyl, cyclohexyl, and phenyl wherein said lower alkyl is unsubstituted or substituted with 1-3 of --OH, Cl, Br, aryl, aryloxy, lower alkanoyloxy, lower alkoxy, or lower alkoxy substituted with --OH, Cl, Br, or lower alkoxy, and wherein said phenyl is unsubstituted or substituted with Cl, Br, lower alkoxy, or lower alkyl, and when X is S, R 1 is further selected from pyridyl, pryimidinyl, benzothiazolyl, benzoxazolyl, benzimidazolyl, azolyl radicals having the formula ##STR33## wherein Y is an oxygen or sulfur atom and Z is an ethylenically unsaturated group of two carbon atoms or of a nitrogen and a carbon atom, wherein said azolyl radicals may be substituted with lower alkyl, phenyl, or phenyl substituted as above for R 1 ; R 2 is selected from hydrogen, lower alkyl, lower alkoxy, formamido, lower alkoxycarbonylamino, lower alkanoylamino, lower alkanoylamino substituted with cyano, lower alkoxy, lower alkoxycarbonyl, phenoxy, or phenyl, phenoxy, halogen substituted phenoxy, cycloalkylcarbonyl, and lower alkylsulfonyl; R 3 is H, or lower alkyl; and R 4 and R 5 are independently selected from H, alkyl of 1-8 carbons, cyclohexyl, phenyl, lower alkoxycarbonyl substituted phenyl, and lower alkyl substituted with cyclohexyl, lower alkanoyloxy, lower alkoxycarbonyl, succinimido, lower alkanoylamino, lower alkylsulfonylamino, lower alkyl sulfonyl, sulfamoyl, carbamoyl, hydroxy, pyrrolidono, phthalimido, aryl, cyano, aryloxy, lower alkoxycarbonyloxy, lower alkoxy, phenoxy, or lower alkoxyalkoxy.
Claim 3
Dependent Claim 9 words
A compound of claim 1 having the formula ##STR34##
Claim 4
Dependent Claim 9 words
A compound of claim 1 having the formula ##STR35##
Claim 5
Dependent Claim 9 words
A compound of claim 1 having the formula ##STR36##
Claim 6
Dependent Claim 9 words
A compund of claim 1 having the formula ##STR37##
Claim 7
Dependent Claim 9 words
A compound of claim 1 having the formula ##STR38##

References Cited (Backward Citations)

US3143540A Cited
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GB1158996A Cited
US3491082A Cited
US3657187A Cited
US3816338A Cited
GB1379233A Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1986-02-21 1986-08-23 1987-02-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1990-02-21 1990-08-23 1991-02-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1994-02-21 1994-08-23 1995-02-22 $7700.00 Window Closed / Lapsed

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