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filingDate 1985-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1987-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 1987-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4660060-A
titleOfInvention Imaging systems containing 3-(indol-3-yl)-3-(4-substituted aminophenyl)phthalides
abstract 3-(1-R-2-R1-5/6-Y-indol-3-yl)-3-(2-R2-4-N-R3-N-R4-aminophenyl)-X-phtha lides, 7-(1-R-2-R1-5/6-Y-indol-3-yl)-7-(2-R2-4-N-R3-N-R4-aminophenyl)furo[3,4 b]-pyridine-5(7H)-ones and 5-(1-R-2-R1-5/6-Y-indol-3-yl)-5-(2-R2-4-N-R3-N-R4-aminophenyl)furo[3,4 b]-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-R1-5/6-Y-indol-3-yl)carbonyl-X-benzoic acid with the corresponding 3-R2-N-R3-N-R4-aniline or the interaction of the corresponding 2-(2-R2-4-N-R3-N-R4-aminophenyl)carbonyl-X-benzoic acid with the corresponding 1-R-2-R1-5/6-Y-indole. The furopyridines are prepared by the interaction of the corresponding 2/3-(1-R-2-R1-5/6-Y-indol-3-yl)carbonylpyridine-3/2-carboxylic acid with the corresponding 3-R2-N-R3-N-R4-aniline. The novel 1-R-2-R1-5/6-Y-indol-3-yl)carbonyl-X-benzoic acids and 1-R-2-R1-5/6-Y-indoles are useful as intermediates to the appropriate phthalides and furopyridinones.
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135817270
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID73773
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21283992
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127894152
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21283994
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14178120
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226502190
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21283999
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127893414
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127882096
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21284000
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393570
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128087197
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21283998
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6461
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID60074860
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID236011082
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128724960
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229407234
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226506897
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22016303
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128400238
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68994
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID104335
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226405793
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21283987
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1018
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Total number of triples: 358.