synthesis, nmr and crystallographic studies of 2-substituted dihydroquinazolinones derived from (s)-phenylethylamine合成、核磁共振以及晶体的研究2-substituted dihydroquinazolinones来自(s)苯乙胺.pdfVIP
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synthesis, nmr and crystallographic studies of 2-substituted dihydroquinazolinones derived from (s)-phenylethylamine合成、核磁共振以及晶体的研究2-substituted dihydroquinazolinones来自(s)苯乙胺
Molecules 2007, 12, 173-182
molecules
ISSN 1420-3049
Full Paper
Synthesis, NMR and Crystallographic Studies of 2-Substituted
Dihydroquinazolinones Derived from (S)-Phenylethylamine
Jaime Escalante 1,*, Claudia Ortíz-Nava 1, Patricia Flores 1, Jaime M. Priego 1 and
Cirilo García-Martínez 2,*
1 Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Morelos. Av.
Universidad No. 1001, Col. Chamilpa, C.P. 62210 Cuernavaca-Mor. México.
2 Universidad Autónoma Metropolitana, Area de Química. San Pablo No. 180, Col. Reynosa
Tamaulipas, México 02200, D.F.
* Authors to whom correspondence should be addressed; E-mails: jaime@ciq.uaem.mx or
gmc@correo.azc.uam.mx
Received: 5 December 2006; in revised form: 2 February 2007 / Accepted: 5 February 2007 /
Published: 12 February 2007
Abstract: 2,3-Dihydro-3-[(S)-1-phenethyl]quinazolinone and some new 2-substituted
derivatives bearing isopropyl, o-nitrophenyl and p -nitrophenyl groups were prepared in
40-90% yield by amidation of isatoic anhydride with (S)-phenylethylamine, followed by
condensation with triethyl orthoformate, isopropylaldehyde, o-nitro- and p -nitro-
benzaldehyde, respectively. The two 2-subtituted dihydroquinazolinones obtained either
by using isopropylaldehyde, o-nitro- or p -nitrobenzaldehyde, were separated and purified
before their NMR spectra in CDCl3 solutions were recorded. The detection of the low
energy conformation of O=C-N-phenethyl segment in solution allowed the correlation of
the NMR data with the configuration of newly stereogenic
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