76315-66-7Relevant articles and documents
Lewis-acid-promoted cyclization reaction: Synthesis of N3-chloroethyl and N3-thiocyanatoethyl quinazolinones
Hu, Fang-Peng,Zhang, Ming-Ming,Huang, Guo-Sheng
, p. 9315 - 9319 (2021/06/14)
A Lewis-acid-promoted cyclization reaction of benzoyl chlorides with 2-(4,5-dihydrooxazol-2-yl)anilines, which can offer a series of N3-chloroethyl quinazolinones, is disclosed. The reaction is compatible with the functional groups of the substrates; environment-friendly AlCl3 is probably the chloride source. Moreover, the addition of NH4SCN can also produce a range of N3-thiocyanatoethyl quinazolinones in moderate-to-good yields.
Studies on quinazolines. 11. Intramolecular imidate-amide rearrangement of 2-substituted 4-(ω-chloroalkoxy)quinazoline derivatives. 1,3 -O → N shift of chloroalkyl groups via cyclic 1,3-azaoxonium intermediates
Chen, Grace Shiahuy,Kalchar, Shivaramayya,Kuo, Chun-Wei,Chang, Chih-Shiang,Usifoh, Cyril O.,Chern, Ji-Wang
, p. 2502 - 2505 (2007/10/03)
The ω-chloroalkylation of 2-substituted quinazo lin-4(3H)-one derivatives 1 and 2 with Br-(CH2)n-Cl (n = 2-4) and the intramolecular imidate-amide rearrangement of the alkylated products are described. At room temperature, the 2-phenyl substituent promoted O-alkylation, whereas the less steric 2-benzyl group led to a higher ratio of N-alkylation. The investigation of the O-alkylated products, 4-ω-chloroalkoxyquinazolines, revealed that the migration of ω-chloroethyl and ω-chloropropyl groups from oxygen to nitrogen should be intramolecular via five- and six-membered cyclic 1,3-azaoxonium intermediates, respectively. Competition between rearrangement and nucleophilic substitution results in the formation of 7a,b and 8a,b from the nucleophilic substitution of 4a,b and 6a,b, respectively.
