http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4316036-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S430-165
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-04
filingDate 1978-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b09981be63b59fa36e7be2c7fd9f9d7
publicationDate 1982-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4316036-A
titleOfInvention Benzopyranothiazoles
abstract A benzopyranothiazole of the formula <IMAGE> (1) wherein each of R1 and R2 independently represents hydrogen, alkyl of not more than 12 carbon atoms which is unsubstituted or substituted by halogen, hydroxyl, cyano or lower alkoxy, or represents cycloalkyl, phenyl, benzyl, or phenyl or benzyl which is substituted by halogen, lower alkyl or lower alkoxy, or R1 and R2 together with the nitrogen atom to which they are attached represent a 5- or 6-membered heterocyclic radical or a N-carbazolyl radical, Q represents hydrogen, lower alkyl, benzyl or groups of the formulae (1a) or (1b) <IMAGE> each of X, X1 and X2 represents hydrogen, halogen, lower alkyl or lower alkoxy, each of Y1, Y2, Y'1 and Y'2 represents hydrogen, alkyl of not more than 12 carbon atoms which is unsubstituted or substituted by halogen, hydroxyl, cyano or lower alkoxy, or represents cycloalkyl, phenyl, benzyl, or phenyl or benzyl which is substituted by halogen, lower alkyl or lower alkoxy, or each of the pair of substituents Y1 and Y2 and Y'1 and Y'2, together with the nitrogen atom to said pair is attached, independently represents a 5- or 6-membered heterocyclic radical or a N-carbazolyl radical and the ring A is unsubstituted or substituted by halogen, nitro, lower alkyl, lower alkoxy, phenoxy or an amino group which is unsubstituted or substituted by lower alkyl, phenyl or benzyl; these compounds are particularly useful as color formers which give intense red to blue color shades of excellent light fastness when they are brought into contact with an electron-accepting co-reactant.
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priorityDate 1977-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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