Imaging systems containing 3-(indol-3-yl)-3-(4-substituted amino

Recorders – Record receiver deforming

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346223, 427151, B41M 516, B41M 518, B41M 522

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active

046600604

ABSTRACT:
3-(1-R-2-R.sup.1 -5/6-Y-indol-3-yl)-3-(2-R.sup.2 -4-N-R.sup.3 -N-R.sup.4 -aminophenyl)-X-phthalides, 7-(1-R-2-R.sup.1 -5/6-Y-indol-3-yl)-7-(2-R.sup.2 -4-N-R.sup.3 -N-R.sup.4 -aminophenyl)furo[3,4b]-pyridine-5(7H)-ones and 5-(1-R-2-R.sup.1 -5/6-Y-indol-3-yl)-5-(2-R.sup.2 -4-N-R.sup.3 -N-R.sup.4 -aminophenyl)furo[3,4b]-pyridine-7(5H)-ones are useful as color formers in transfer imaging systems, pressure-sensitive carbonless duplicating systems and thermal-responsive marking systems. The phthalides are prepared by the interaction of the corresponding 2-(1-R-2-R.sup.1 -5/6-Y-indol-3-yl)carbonyl-X-benzoic acid with the corresponding 3-R.sup.2 -N-R.sup.3 -N-R.sup.4 -aniline or the interaction of the corresponding 2-(2-R.sup.2 -4-N-R.sup.3 -N-R.sup.4 -aminophenyl)carbonyl-X-benzoic acid with the corresponding 1-R-2-R.sup.1 -5/6-Y-indole. The furopyridines are prepared by the interaction of the corresponding 2/3-(1-R-2-R.sup.1 -5/6-Y-indol-3-yl)carbonylpyridine-3/2-carboxylic acid with the corresponding 3-R.sup.2 -N-R.sup.3 -N-R.sup.4 -aniline. The novel 1-R-2-R.sup.1 -5/6-Y-indol-3-yl)carbonyl-X-benzoic acids and 1-R-2-R.sup.1 -5/6-Y-indoles are useful as intermediates to the appropriate phthalides and furopyridinones.

REFERENCES:
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patent: 3775424 (1973-11-01), Farber
patent: 4062866 (1977-12-01), Garner et al.
patent: 4349679 (1982-09-01), Garner et al.
patent: 4399209 (1983-08-01), Sanders
patent: 4508897 (1985-12-01), Bedekovic et al.

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