Structural characterization of prazosin hydrochloride and prazosin free base
β Scribed by Chernyshev, Vladimir V. (author);Stephens, Peter W. (author);Yatsenko, Alexandr V. (author);Ryabova, Olga B. (author);Makarov, Vadim A. (author)
- Publisher
- John Wiley and Sons Inc.
- Year
- 2004
- Tongue
- English
- Weight
- 121 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0022-3549
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β¦ Synopsis
The three-dimensional solid-state structures of prazosin hydrochloride, C 19 H 22 N 5 O 4 ΓΎ Γ Cl Γ (A), and prazosin free base, C 19 H 21 N 5 O 4 (B), have been determined by synchrotron X-ray powder diffraction. A and B crystallize in triclinic P-1 and monoclinic Cc space groups, respectively, with one structural unit per asymmetric part. In A and B, the prazosin molecule adopts different conformations, which do not correspond to those obtained by DFT optimizations of protonated and free prazosin.
π SIMILAR VOLUMES
Treatment of the enamine 2, formed by condensation of 2indanone and ethyl(2-methallyl)amine, with n-butyllithium yields 2-[ethyl(2-methallyl)amino]indenyllithium (3), whose structure was determined by X-ray single crystal diffraction. Complex 3 exhibits an oligomeric supersandwich structure