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<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Iranian Journal of Catalysis</JournalTitle>
<Issn>2345-4865</Issn>
<Volume>6</Volume>
<Issue>4</Issue>
<PubDate PubStatus="epublish">
<Year>2024</Year>
<Month>02</Month>
<Day>03</Day>
</PubDate>
</Journal>
<ArticleTitle>Thiamine hydrochloride (vitamin B1) as an efficient catalyst for the synthesis of 4-(3H)-Quinazolinone derivatives using grinding method.</ArticleTitle>
<VernacularTitle></VernacularTitle>
<FirstPage></FirstPage>
<LastPage></LastPage>
<ELocationID EIdType="doi"></ELocationID>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Deepak S.</FirstName>
<LastName>Kawade</LastName>
<Affiliation>Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad - 431004, Maharashtra, India.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Mahendra A.</FirstName>
<LastName>Chaudhari</LastName>
<Affiliation>Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad - 431004, Maharashtra, India.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Jitendra B.</FirstName>
<LastName>Gujar</LastName>
<Affiliation>Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad - 431004, Maharashtra, India.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Murlidhar S.</FirstName>
<LastName>Shingare</LastName>
<Affiliation>Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431004 (MS) India.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
</AuthorList>
<PublicationType>Journal Article</PublicationType>
<History>
<PubDate PubStatus="received">
<Year>2024</Year>
<Month>02</Month>
<Day>03</Day>
</PubDate>
</History>
<Abstract>Herein we explore facile synthesis of 4-(3H)-Qunazolinone derivatives, achieved by the cyclocondensation of anthranilic acid, aromatic amines and triethyl orthoformate in presence of thiamine hydrochloride (Vitamin B1) as a catalyst, using grinding method. This protocol offers several advantages such as reusability of catalyst, excellent yield, shorter reaction time and economic availability.Quinazolinone derivatives are one of the most important class of biodynamic heterocycles due to their wide range of biological activities such as anticancer [1], antitubercular agent [2], anti-inflammatory and antioxidant [3], anticonvusant agent [4], antimicrobial [5], antitumor [6], ACHE inhibitor [7], antiviral [8] and calcilytic activities [9-10]. Owing to the broad range of pharmacological, biological activities and development of new method for synthesis of quinazolinones derivative is still desirable.</Abstract>
<ObjectList>
<Object Type="keyword">
<Param Name="value">4-(3H)-Quinazolinones</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Anthranilic acid</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Multi-component reaction</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Thiamine hydrochloride (VB1)</Param>
</Object>
</ObjectList>
</Article>
</ArticleSet>