Reaction of 2-Aminobenzohydrazides with Schiff Bases. A New Route to 3-Benzylideneamino-4(3H)-quinazolinones and 2--5-aryl-1,3,4-oxadiazoles

DOI: 10.1246/bcsj.59.1575

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1575 - 1580 (1986)

Update date:2022-07-29

Topics: Synthesis Cyclization Structural characterization Product Isolation Condensation Reaction Reaction Optimization Schiff Bases 1,3,4-oxadiazoles

Authors:

Pratap Reddy, Padi

Kista Reddy, Cheppala

Satyanarayana N. Reddy, Padala

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Article abstract of DOI:10.1246/bcsj.59.1575

Reaction of 2-aminobenzohydrazides with Schiff bases in methanol followed by KMnO4 oxidation has resulted in the presence formation of 3-benzylideneamino-4(3H)-quinazolinones and 2-<2-(methylamino)phenyl>-5-aryl-1,3,4-oxadiazoles, characterized by spectra

Full text of DOI:10.1246/bcsj.59.1575

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Product name:N-(4-methoxy-benzyliden)-anthranilic acid-(4-methoxy-benzylidene-hydrazide)

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