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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>1</Volume><Issue>2</Issue></Journal><ArticleTitle>Preparation of Novel Acylguanidines with Potential H2 -Blocking Activity</ArticleTitle><FirstPage>115</FirstPage><LastPage>120</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Jalal Hanaee</LastName></Author><Author><FirstName></FirstName><LastName>M. Reza Rashidi</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>3- chlorocyclohex-2-enone(2) was obtained directly by reaction of cyclohex-1,3-dione with triphyenylphosphine in CCl . Guanidine hydrochloride was treated with sodium methoxide to give the free base. The free base was treated with 3- chloro-cyclohex-2-enone (2) in methanol and yielded the acylguanidine (3). Also reaction of 5,5-dimethyl-3-methoxycyclohex-2~enone (8) with 2- amino-1,4,5,6- tetrahydro-pyrimidine (9) in isopropanol gave 2- (5,5-dimethyl-3-oxocyclohex-2-enylamine)~ 1,4,5,6-tetrahydropyrimidine (10). They both can be considered as new lead compounds with potential H -blocking activity. Further investigation will be needed to prepare modified strctures and effective H -blockers and evaluate their properties.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/16</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/16/16</pdf_url></Article></Articles>
