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http://dx.doi.org/10.5352/JLS.2004.14.1.091

Synthesis of N-acyl-α-aminosuccinimides and N-acyl-α-aminoglutarimides  

정대일 (동아대학교 화학과)
김문주 (동아대학교 화학과)
송현애 (동아대학교 화학과)
김윤영 (동아대학교 화학과)
이용균 (동아대학교 화학과)
박유미 (동아대학교 화학과)
최순규 (동아대학교 화학과)
한정태 (영동대학교 화학과)
박민수 (경성대학교 약학과)
Publication Information
Journal of Life Science / v.14, no.1, 2004 , pp. 91-97 More about this Journal
Abstract
As a part of our study on the improvement of anticonvulsant, here we report the synthesis of N-acyl-$\alpha$-aminosuc-cinimides 1 and N-acyl-$\alpha$-aminoglutarimides 2. (R)-Benzoic acid 4-benzyloxycarbonylamino-2-oxo-pyrrolidin-1-ylester 6a, (R)-4-nifro-benzoic acid 4-benzyloxycarbonylamino-2- oxo-pyrrolidin-1-yl ester 6b, (R) -4-nitro-benzoic acid 4-benzyloxycarbonylamino-2-oxo-pyrrolidin-1-yl ester 6c, and (R)-propionic acid 4-benzyloxycarbonylamino-2-oxo-pyrrolidin-1-yl ester 6d were synthesized from (R)-2-benzyloxy carbonylamino-succinic acid 3 as a starting meterial. (R)-(3- Benzyloxycarbonylamino-2,6-dioxo-piperidin-1-yloxy)-acetic acid methyl ester 10a, (R)-(3-benzyloxycarbonylamino-2,6-dioxo-piperidin-1-yloxy)-acetic acid ethy1 ester 10b, an d (R)-2-(3-benzyloxycarbonylamino-2,6- diox o-piperidin-1-yl oxy)-propionic acid methyl ester l0c were synthesized from (R)- 3-carbobenzyloxy-amino-glutarmic acid 7 as a starting meterial. The yield, mp, IR, $^1H-NMR,\; and^{13}C$- NMR spectra of the products 6a, 6b, 6c, 6d, 10a, l0b, l0c are summarized in footnote. The biological studies of these compounds are in progress and will be reported in future.
Keywords
anticonvulsant; N-acyl-$\alpha$-aminosuccinimides; N-acyl-$\alpha$-aminoglutarimides; ME test; PTZ test;
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