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Design and Synthesis of Novel 2-Trichloromethyl-4-Substituted Quinazoline Derivatives as Anti-tubercular Agents

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1TitleTitle of DocumentDesign and Synthesis of Novel 2-Trichloromethyl-4-Substituted Quinazoline Derivatives as Anti-tubercular Agents
2CreatorAuthor's name, affiliation, country MANEESH KUMAR SRIVASTAV and S. M. SHANTAKUMAR*
Department of Pharmaceutical Chemistry, V. L. College of Pharmacy, Raichur-584103, Karnataka, India
3SubjectDicipline(s) Chemical Science
3SubjectKeywords Anti-tubercular activity, 2-Trichloromethyl quinazoline, Acetylation
4DescriptionAbstract In order to produce a new lead for anti-tubercular drug a series of novel 2-trichloromethyl quinazoline derivatives bearing substituted secondary amine group at the 4th position were designed, synthesized and evaluated for their in vitro anti-tubercular activity against bacterial strain of M. tuberculosis H37Rv ATCC (American Type Culture Collection) by Alamar Blue assay method (MABA). The targeted molecules (4a-j) were synthesized from 4-chloro-2-(trichloromethyl) quinazoline and substituted secondary amine in dichloromethane using catalytic amount of KI, under reflux for 15-18 h. All the targeted compounds are new chemical entities and obtained in satisfactory yields and the structure of the synthesized compounds are in agreement with spectral data. Compound 4a and 4f exhibited potent anti-tubercular activity against bacterial strain of M. tuberculosis H37Rv, with MIC value 6.25 μG.
5PublishersOrganizing agency, location WWW Publications, India
6Contributor Sponsor(s) -
7DateDate (YYYY-MM-DD) -
8TypeStatus & genre Peer-reviewed Article
8TypeType
9FormateFile Formate PDF
10IdentifierUniform Resource Identifier Click Here
10IdentifierDigital Object Identifier
11SourceJournal/conference title; vol., no. (Year)Chemical Science Transactions, Volume  2 , Number  (3), (2013)
12LanuguageEnglish=en en
13RelationSupp.files
14Coverage -
15CopyrightCopyright and permissions
Chemical Science Transactions | Chem Sci Trans | CST | Online Chemistry Journal | Open Access
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