(1 S ,3 R )- N -{(3 S ,10 S ,12 S ,13 R ,17 R )-12-Hy-droxy-17-[( R )-5-hy-droxy-pentan-2-yl]-10,13-di-methyl-hexa-deca-hydro-1 H -cyclo-penta-[ a ]phenanthren-3-yl}adamantane-1-carboxamide 0.25-hydrate
The title compound, C H NO ·0.25H O, was synthesized from de-oxy-cholic acid followed by a protection, a Mitsonobu substitution, a Staudinger reduction, formation of an amide and final reduction in the lateral chain. The compound crystallizes in the 1 space group with four steroid mol-ecules and one...
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Veröffentlicht in: | IUCrData 2022-10, Vol.7 (Pt 10), p.x220947, Article x220947 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The title compound, C
H
NO
·0.25H
O, was synthesized from de-oxy-cholic acid followed by a protection, a Mitsonobu substitution, a Staudinger reduction, formation of an amide and final reduction in the lateral chain. The compound crystallizes in the
1 space group with four steroid mol-ecules and one water mol-ecule in the triclinic cell unit. The crystal structure features O-H⋯O hydrogen bonding. The crystal studied was refined as a non-merohedral twin. |
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ISSN: | 2414-3146 2414-3146 |
DOI: | 10.1107/S2414314622009476 |