Optimized Synthesis of New N-Mustards Based on 2-Mercaptobenzoxazole Derivatives with Antitumor Activity

基于具有抗肿瘤活性的2-巯基苯并恶唑衍生物的新型N-芥子气的优化合成

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作者: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

Abstract

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 Ehrlich Ascites in an appreciable proportion compared to the drug I.O.B.-82, as our studies evidenced.

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