2002
DOI: 10.2298/jsc0211719p
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Disperse dyes based on 2-methyl-3-[3’-amino-phthalimido]-4(3H)-quinazilinone

Abstract: A series of new heterocyclic disperse dyes has been prepared by subsequent diazotization of 2-methyl-3-[3?-aminophthalimido]-4(3H)-quinazolinone and coupling with various mono- and di-N-substituted derivatives of aniline. All the disperse dyes were characterized by their percentage yield, melting point, UV-visible spectrum, elemental analysis, infrared spectrum and dyeing performance on nylon 66 and polyester fibres. The percentage dye bath exhaustion on different fibres was found to be reasonably good and acc… Show more

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Cited by 3 publications
(2 citation statements)
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“…These values are slightly higher than the spin value (1.73 B.M.) expected for one unpaired electron, indicating octahedral geometry around Cu(II) [34]. The magnetic moment value of the heterotrinuclear complex (III), which contains two Cu(II) ions, is 2.54 B.M.…”
Section: Electronic Spectra and Magnetic Moments Of The Complexesmentioning
confidence: 67%
“…These values are slightly higher than the spin value (1.73 B.M.) expected for one unpaired electron, indicating octahedral geometry around Cu(II) [34]. The magnetic moment value of the heterotrinuclear complex (III), which contains two Cu(II) ions, is 2.54 B.M.…”
Section: Electronic Spectra and Magnetic Moments Of The Complexesmentioning
confidence: 67%
“…Zentmayer and Wagner developed a convenient and fairly general procedure for preparation of acylanthranils or 3,1,4benzoxazinone (Zentmayer et al 1949). 2-Amidobenzoic acid on refluxing with acetic anhydride yield benzoxazinone, which reacts exothermally with ammonia and most amine in aqueous media to give high yield of quinazolin-4(3H)ones (Zhou et al 2004, Patel et al, 2002, Parmar et al, 1968. Reactions of substituted aromatic amine with acetanthranil have been extensively studied (Erred et al, 1976(Erred et al, , 1977a(Scheme 15).The synthetic methodology commence with the synthesis of anthranil amide by the oxidation of 2-amino benzonitrile, followed by its amidation using acid chloride and triethylamine to give the uncyclized amide intermediate, which on oxidative ring closure under basic conditions, using potassium hydroxide yield 2substituted-quinazolin-4(3H)ones (Roy et al, 2006, Witt et al, 2000, Bergman et al, 1990) (Scheme 16).…”
Section: 4-disubstituted Quinazolinesmentioning
confidence: 99%