Structure Information
Structure

Compound Identification

SMILES

CC1=CC2=C(C=C1)C(=N\C(N2)=C1/C=CC=CC1=O)N1CCN(CC1)C(=O)C(O)CCl

InChIKey

InChIKey=NIAZZNHCJBEMAC-CAPFRKAQSA-N

Formula

C22H23ClN4O3

Mass

426.9

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Diazanaphthalenes

Subclass

Benzodiazines

Intermediate Tree Nodes

Quinazolines

Direct Parent

Quinazolinamines

Alternative Parents

O-quinomethanes Benzenoids Imidolactams Piperazines Vinylogous amides Tertiary carboxylic acid amides Secondary alcohols Chlorohydrins Ketene acetals Propargyl-type 1,3-dipolar organic compounds Carboximidamides Carboxamidines Azacyclic compounds Hydrocarbon derivatives Amines Alkyl chlorides Organochlorides Organic oxides

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Quinazolinamine - O-quinomethane - Quinomethane - 1,4-diazinane - Imidolactam - Benzenoid - Piperazine - Vinylogous amide - Tertiary carboxylic acid amide - Carboxamide group - Chlorohydrin - Halohydrin - Ketene acetal or derivatives - Ketone - Cyclic ketone - Secondary alcohol - Amidine - Carboxylic acid amidine - Carboxylic acid derivative - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Organic nitrogen compound - Alkyl chloride - Amine - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as quinazolinamines. These are heterocyclic aromatic compounds containing a quianazoline moiety substituted by one or more amine groups.

External Descriptors

Not available

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