The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 27, 1978

Filed:

Apr. 03, 1974
Applicant:
Inventor:

Daniel Shaw James, Hockessin, DE (US);

Assignee:
Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C09B / ; C09B / ; C09B / ;
U.S. Cl.
CPC ...
260157 ; 260154 ; 260156 ; 260160 ; 260162 ; 260163 ;
Abstract

Azo dyes free of water solubilizing groups having the formula ##STR1## WHEREIN R.sub.1 is C.sub.1-4 alkyl, --CH.sub.2 --CH.dbd.CH.sub.2, ##STR2## --(CH.sub.2).sub.n R.sub.8, C.sub.1-4 alkyleneCN, C.sub.2 H.sub.4 OR.sub.7, --CH.sub.2 --CH.dbd.CH--R.sub.8, --C.sub.2 H.sub.4 CONH.sub.2, --C.sub.2 H.sub.4 CONHC.sub.1-4 alkyl, --C.sub.2 H.sub.4 CON(C.sub.1-4 alkyl).sub.2 and --C.sub.2 H.sub.4 CO.sub.2 C.sub.1-4 alkyl; A is a coupling component selected from: a 5- or 6-membered heterocycle consisting of 5-aminopyrazole, 5-pyrazolone, barbituric acid, 6-hydroxypyrid-2-one, 4-hydroxycoumarin and 1,2-dialkylindole; a 1- or 2-naphthol group and an aromatic amine of the formula ##STR3## W is 1,4-naphthylene or ##STR4## R.sub.2 is H, F, Cl, C.sub.1-4 alkyl, OC.sub.1-4 alkyl; R.sub.3 is cyclohexyl or C.sub.1-14 alkylene-R.sub.9 ; R.sub.2 and R.sub.3 together with the nitrogen atom optionally form a 6-membered ring optionally substituted with --OH, OC.sub.2 H.sub.4 CN or OCOC.sub.1-5 alkyl; R.sub.4 is H, ##STR5## R.sub.3 and R.sub.4 together optionally form a 6-membered heterocyclic ring containing the nitrogen atom; R.sub.5 is H; R.sub.6 is H, F, Cl, Br, C.sub.1-4 alkyl, OC.sub.1-4 alkyl, OH, C.sub.1-4 hydroxyalkyl, NHCOCH.dbd.CH.sub.2, NHCOC.sub.1-4 alkyl, NHCOR.sub.8, NHCO.sub.2 C.sub.1-4 alkyl, NHCONHC.sub.1-4 alkyl, NHSO.sub.2 C.sub.1-4 alkyl, NHSO.sub.2 R.sub.8, NHCO.sub.2 R.sub.8, NHCONHR.sub.8, NHCOC.sub.1-4 alkylene-R.sub.10, NHCOC.sub.1-4 alkylene-OC.sub.1-4 alkylene-R.sub.10, NHCO.sub.2 C.sub.11-4 alkyleneOC.sub.1-4 alkyl; R.sub.5 and R.sub.6 together optionally form --CH.dbd.CH--CH.dbd.CH--; R.sub.7 is H or C.sub.1-4 acyl; R.sub.8 is phenyl or phenyl optionally substituted with 1-2 groups selected from Cl, Br, CN, CF.sub.3, NO.sub.2, C.sub.1-4 alkyl, OC.sub.1-4 alkyl, N(C.sub.1-4 alkyl).sub.2 and NHCOC.sub.1-4 alkyl; R.sub.9 is H, OH, CN, COC.sub.1-4 alkyl, OCOCH.dbd.CH.sub.2, OCOC.sub.1-4 alkylene-R.sub.11, OCOR.sub.8, CO.sub.2 R.sub.8, CO.sub.2 C.sub.1-4 alkylene-R.sub.12, ##STR6## OC.sub.1-4 alkylene-R.sub.10, CONHC.sub.1-4 alkylene-R.sub.11, SO.sub.2 R.sub.8, OCONHC.sub.1-4 alkylene-R.sub.10, NHCOC.sub.1-4 alkylene-R.sub.10, NHCONHR.sub.8, NHCOR.sub.8 or R.sub.8 ; R.sub.10 is CN, OH, Cl, Br or R.sub.7 ; R.sub.11 is H, Cl, Br, OC.sub.1-4 alkyl or phenyl; R.sub.12 is H, OH, OC.sub.1-4 alkyl, OCOC.sub.1-4 alkylene-R.sub.11 or OCOR.sub.8 ; R.sub.13 and R.sub.14 are independently H, C.sub.1-4 alkyl, C.sub.1-4 alkyl, C.sub.1-4 alkoxy or Cl; m is 0 or 1; and n is 1 to 3.


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