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Optimized Synthesis of New N-Mustards Based on 2-Mercaptobenzoxazole Derivatives with Antitumor Activity
oleh: Corina Cheptea, Valeriu Sunel, Ana Cezarina Morosanu, Dan Gheorghe Dimitriu, Mihaela Maria Dulcescu-Oprea, Mihai-Daniel Angheluta, Mihaela Miron, Cristina Delia Nechifor, Dana Ortansa Dorohoi, Razvan Nicolae Malancus
| Format: | Article |
|---|---|
| Diterbitkan: | MDPI AG 2021-04-01 |
Deskripsi
New di-(β-chloroethyl)-amides of some acids derived from 2-mercaptobenzoxazole were prepared by reaction of the corresponding pivalic mixed anhydrides with di-(β-chloroethyl)-amine. A study regarding the optimization of the chemical reactions was made for the case of di-(β-chloroethyl)-amines. The quantum chemical analysis by Spartan’14 was made in order to establish the most stable configuration of the ground electronic states for the obtained chemical structures and some physico-chemical parameters of N-mustards reported in this paper. Mercaptobenzoxazoles substituted in the side chain with the cytotoxic group show antitumor activity and they inhibit <i>Ehrlich Ascites</i> in an appreciable proportion compared to the drug I.O.B.-82, as our studies evidenced.