I. The quinazolines, a branch of the benzodiazine class of aromatic nitrogen hetercycles, do not occur to any great extent in naturally occurring compounds. The discovery of the antimalarial febrifugine and its structure elucidation led to the preparation and investigation of a host of new quinazolines in the search for new and more effective antimalarials. Most of the present body of information governing the quinazolines arose out of these synthetic studies. The present study has been accomplished with a four-fold purpose in mind: (1) to investigate the susceptibility of chloroquinazolines to nucleophilic displacement reactions by thiols or their salts, (2) to expand the present body of knowledge concerning the chemistry of the quinazolines, (3) to investigate the susceptibility of sulfides of quinazolines to oxidation to sulfoxides and sulfones, and (4) to prepare new compounds of potential chemotherapeutic value. A procedure for the preparation of 4-chloroquinazoline was worked out and thiol displacements were carried out on this material as well as the 2,4-dichloroquinazoline and 2-chloro-4(3H)-quinazolinone. Twenty-six new thioethers were prepared. Oxidation of these thioethers yielded the oxo derivatives in all but two instances. 4-Methylthioquinazoline was oxidized to 2(1H)-oxoquinazoline- 4-sulfonic acid and 4-phenylthioquinazoline yielded the 2(1H)-oxo-4-phenylsulfinylquinazoline. 4(3H)-Quinazolinethione when treated with dimethyl-sulfate yielded the 1-methyl derivative. When 2-benzyl-thio- 4(3H)-quinazolinone was treated with dimethyl sulfoxide it was converted into 2-benzylthio-3-methylthio-4- quinazolinone. 4-n-Butylthioquinazoline, when treated with per-benzoic acid, yielded 3-(4'-quinazolyl)-4(3H)-quinazolinone. II. Investigations on 2-chloromethyl-4-methyl-quinazoline 3-oxide using primary amines yielded the simple displacement products. Work carried out on 6-chloro- 2-chloromethyl-4-phenylquinazoline 3-oxide with primary amine displacements yielded the simple products and also a ring expanded 1,4-benzodiazepine 4-oxide. This phase of the investigation has been carried out with the following purposes in mind: (1) to examine the conditions under which 6-chloro-2-chloromethyl-4- phenylquinazoline 3-oxide and related analogs rearrange to the 1,4-benzodiazepine 4-oxide, (2) to determine if a similar rearrangement will occur when thiols are used, (3) to investigate the possible rearrangement of the amine and thiol displacement products of 2-chloromethyl- 4-methylquinazoline 3-oxide and the 6-bromo analog, and (4) to examine the possible rearrangement of the 2-alkyl-aminomethylquinazolines. Although a number of conditions were employed, the aminomethylquinazolines were found not to rearrange to the diazepines. Thiol displacements yielded the simple displacement products in each case studied. Amine displacements on 2-chloromethyl-4-methylquinazoline 3- oxides yield simple displacement products. With the 6-bromo-2-chloromethyl-4-methylquinazoline 3-oxide and simple amines the diazepine is formed. Dilute solutions of both the quinazolines and the diazepines change on standing in daylight at room temperature but the products have not been identified.
College and Department
Physical and Mathematical Sciences; Chemistry and Biochemistry
BYU ScholarsArchive Citation
Kuchar, Marvin C. J., "I. Preparation and properties of alkyl and aryl substituted thioquinazolines and sulfoxides ; II. An investigation of the quinazoline 3-oxide--1,4-benzodiazepine 4-oxide rearrangement" (1963). Theses and Dissertations. 8294.
Quinazoline, Chemistry, Organic